4-(4-haloalkyl-3-thiobenzoyl)pyrazoles and use thereof as herbicides

ABSTRACT

A description is given of 4-(4-haloalkyl-3-thiobenzoyl)pyrazoles of the formula (I) and of their use as herbicides. 
     
       
         
         
             
             
         
       
     
     In this formula (I), X, Y, R 1 , R 2 , R 3 , and R 4  are radicals such as hydrogen and organic radicals such as alkyl.

CROSS REFERENCE TO RELATED APPLICATIONS

This application claims priority to EP 10170238.9 filed Jul. 21, 2010, the content of which is incorporated herein by reference in its entirety.

BACKGROUND

1. Field of the Invention

The invention relates to the technical field of herbicides, more particularly that of herbicides for the selective control of broadleaf and grass weeds in crops of useful plants.

2. Description of Related Art

From various publications it is already known that certain benzoylpyrazoles possess herbicidal properties. For instance, EP 0 352 543, WO 00/03993, and WO 2008/125214 disclose benzoylpyrazoles substituted by various radicals.

The herbicidal activity of the compounds known from these publications, however, is frequently inadequate. It is therefore an object of the present invention to provide herbicidally active compounds whose herbicidal properties are improved as compared with those of the compounds known from the prior art.

SUMMARY

It has now been found that certain 4-benzoylpyrazoles whose phenyl ring carries a thio group in position 3 and a haloalkyl group in position 4 are especially suitable as herbicides. The present invention firstly provides 4-(4-haloalkyl-3-thiobenzoyl)pyrazoles of the formula (I) or salts thereof.

in which

-   X is (C₁-C₄)-alkyl, -   Y is (C₁-C₄)-haloalkyl or trifluoromethyl, -   R¹ is (C₁-C₄)-alkyl, -   R² is (C₁-C₄)-alkyl, -   R³ is hydrogen or (C₁-C₄)-alkyl, -   R⁴ is hydrogen, (C₁-C₆)-alkylsulfonyl,     (C₁-C₄)-alkoxy-(C₁-C₆)-alkylsulfonyl, or is phenylsulfonyl,     thiophenyl-2-sulfonyl, benzoyl, benzoyl-(C₁-C₆)-alkyl or benzyl,     each of which is substituted by m identical or different radicals     from the group consisting of halogen, (C₁-C₄)-alkyl, and     (C₁-C₄)-alkoxy, -   m is 0, 1, 2 or 3, and -   n is 0, 1 or 2.

DETAILED DESCRIPTION OF A PREFERRED EMBODIMENT

Where R⁴ is hydrogen, the compounds of the invention of the formula (I) may exist in the form of different tautomeric structures, depending on external conditions, such as solvent and pH, as follows:

Depending on the nature of the substituents, the compounds of the formula (I) contain an acidic proton which can be removed by reaction with a base. Examples of suitable bases include hydrides, hydroxides, and carbonates of lithium, sodium, potassium, magnesium, and calcium, and also ammonia and organic amines such as triethylamine and pyridine. In addition, salts may be formed by reaction with organic acids, such as formic acid or acetic acid, and with inorganic acids, such as phosphoric, hydrochloric or sulfuric acid. Such salts are likewise provided by the invention.

In the formula (I) and all subsequent formulae, alkyl radicals having more than two carbon atoms may be straight-chain or branched. Alkyl radicals are, for example, methyl, ethyl, n- or iso-propyl, n-, iso-, tert- or 2-butyl, pentyl, hexyl, such as n-hexyl, iso-hexyl and 1,3-dimethylbutyl. Halogen is fluorine, chlorine, bromine or iodine.

Where a group is substituted multiply by radicals, this means that the group in question is substituted by one or more identical or different members from among the radicals specified.

Depending on the nature and attachment of the substituents, the compounds of the formula (I) may be present in the form of stereoisomers. Where, for example, one or more asymmetrically substituted carbon atoms or sulfoxides are present, then enantiomers and diastereomers may occur. Stereoisomers may be obtained from the mixtures resulting from the preparation process by customary separation methods, such as by chromatographic separation methods, for example. It is likewise possible for stereoisomers to be prepared selectively through deployment of stereoselective reactions using optically active starting materials and/or auxiliaries. The invention also relates to all of the stereoisomers and mixtures thereof that are embraced by the formula (I) but not defined specifically.

Of particular interest are compounds of the formula (I) in which

-   X is (C₁-C₄)-alkyl, -   Y is (C₁-C₄)-haloalkyl or trifluoromethyl, -   R¹ is (C₁-C₄)-alkyl, -   R² is (C₁-C₄)-alkyl, -   R³ is hydrogen or (C₁-C₄)-alkyl, -   R⁴ is hydrogen, (C₁-C₆)-alkylsulfonyl,     (C₁-C₄)-alkoxy-(C₁-C₆)-alkylsulfonyl, or is phenylsulfonyl,     thiophenyl-2-sulfonyl, benzoyl, benzoyl-(C₁-C₆)-alkyl or benzyl,     each of which is substituted by m identical or different radicals     from the group consisting of halogen, (C₁-C₄)-alkyl, and     (C₁-C₄)-alkoxy, -   m is 0, 1, 2 or 3, and -   n is 0, 1 or 2.

Preference is given to compounds of the formula (I) in which

-   X is (C₁-C₄)-alkyl, -   Y is trichloromethyl, difluoromethyl, dichlorofluoromethyl,     chlorodifluoromethyl, pentafluoroethyl or heptafluoroisopropyl, -   R¹ is (C₁-C₄)-alkyl, -   R² is (C₁-C₄)-alkyl, -   R³ is hydrogen or (C₁-C₄)-alkyl, -   R⁴ is hydrogen, n-propylsulfonyl, methoxyethylsulfonyl,     phenylsulfonyl, 4-methyl-phenylsulfonyl, or thiophenyl-2-sulfonyl,     and -   n is 0, 1 or 2.

Particular preference is given to compounds of the formula (I) in which

-   X is methyl, -   Y is difluoromethyl or pentafluoroethyl, -   R¹ is methyl, -   R² is methyl, -   R³ is hydrogen or methyl, -   R⁴ is hydrogen, and -   n is 1 or 2.

Very particular preference is given to compounds of the formula (I) in which

-   X is methyl, -   Y is pentafluoroethyl, -   R¹ is methyl, -   R² is methyl, -   R³ is hydrogen or methyl, -   R⁴ is hydrogen, and -   n is 1 or 2.

In all formulae given below, the substituents and symbols, unless defined otherwise, have the same meaning as described under formula (I).

Compounds of the invention in which R⁴ is hydrogen may be prepared, for example, by the process, indicated in Scheme 1 and known from Acta Chem. Scand. 13 (1959), 1668-1670, by base-catalyzed reaction of a benzoyl halide (III) with a pyrazolone (II), or in accordance with the process indicated in Scheme 2 and known, for example, from EP-A 0 186 117, by base-catalyzed reaction of a benzoyl halide (III) with a pyrazolone (II) and subsequent rearrangement. These processes are also known from WO2005/122768.

The intermediate (IV) may also be prepared by direct reaction of a benzoic acid (IIIa) with a pyrazolone (II) with the addition of an activating condensation agent such as N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride, for example.

Compounds of the invention in which R⁴ has a definition other than hydroxyl are usefully prepared from the compounds obtainable in accordance with Scheme 1 or 2, by alkylation or acylation. Methods of this kind are fundamentally known to the skilled person and described in WO2005/122768, for example.

The pyrazolones of the formula (II) are available commercially or can be prepared in accordance with the process known to the skilled person and described in EP-A 240 001, for example.

The benzoyl halides of the formula (III) are prepared from the benzoic acids of the formula (IIIa) by means, for example, of reaction with thionyl chloride.

The benzoic acids (IIIa) are obtainable via a series of synthetic steps known per se to the skilled person.

For example, the synthesis of benzoic acids carrying a trifluoromethyl group as haloalkyl group in position 4 is known from WO 2008125214. Depending on the nature of the haloalkyl group, the processes described therein may be applied to the synthesis of the benzoic acids (IIIa).

A further possibility is the introduction of haloalkyl groups. For example, the introduction of a pentafluoroethyl group into position 4 of a benzonitrile is described in WO 2006/43064 and US 2007/185058. The benzonitrile may be converted subsequently into the corresponding benzoic acid (US 2007/185058). Also known is the substitution of the iodoaromatic compound by a haloalkyl group, a reaction which proceeds via the corresponding haloalkyl copper compound (A. A. Kolomeitsev et al., J. Org. Chem. 2008, 73 (7), 2607.).

Alternatively, haloalkyl groups may also be generated from other functional groups. A difluoromethyl group is accessible, for example, from the corresponding formyl group. A transformation of this kind is described for 4-formylbenzonitrile by C. P. Andrieux et. al. (Journal of the American Chemical Society 1997 (119), 40, 9527). The corresponding benzoic acid can then be generated from the product under basic conditions, for example (F. Mathey et. al., Tetrahedron 1975 (31), 391.).

Further possibilities for synthetic access to benzoic acids that may be applied to the synthesis of the benzoic acids (IIIa) are known from WO 03/014071.

The sulfur atom in position 3 of the benzoyl group need not necessarily be oxidized at the stage of the benzoic acid in order to generate compounds with n=1 or 2; for example, an oxidation of this kind at the stage of the enol ester or of the 4-benzoyl-5-hydroxypyrazole may also be useful.

Benzoic acids of the formula (IIIa) are new and likewise provided by the invention.

Collections of compounds of the formula (I) and/or salts thereof which can be synthesized by the aforementioned reactions can also be prepared in a parallel manner, it being possible for this to take place in a manual, partly automated or completely automated manner. In this connection, it is, for example, possible to automate the reaction procedure, the work-up or the purification of the products and/or intermediates. Overall, this is understood as meaning a procedure as described, for example, by D. Tiebes in Combinatorial Chemistry—Synthesis, Analysis, Screening (editor Gunther Jung), Verlag Wiley 1999, on pages 1 to 34.

For the parallel reaction procedure and work-up, it is possible to use a series of commercially available instruments, for example Calypso reaction blocks from Barnstead International, Dubuque, Iowa 52004-0797, USA or reaction stations from Radleys, Shirehill, Saffron Walden, Essex, CB11 3AZ, England or MultiPROBE automated workstations from Perkin Elmer, Waltham, Mass. 02451, USA. For the parallel purification of compounds of the formula (I) and salts thereof or of intermediates produced during the preparation, there are available, inter alia, chromatography apparatuses, for example from ISCO, Inc., 4700 Superior Street, Lincoln, Nebr. 68504, USA.

The apparatuses listed lead to a modular procedure in which the individual process steps are automated, but between the process steps manual operations have to be carried out. This can be circumvented by using partly or completely integrated automation systems in which the respective automation modules are operated, for example, by robots. Automation systems of this type can be acquired, for example, from Caliper, Hopkinton, Mass. 01748, USA.

The implementation of single or several synthesis steps can be supported through the use of polymer-supported reagents/scavenger resins. The specialist literature describes a series of experimental protocols, for example in ChemFiles, Vol. 4, No. 1, Polymer-Supported Scavengers and Reagents for Solution-Phase Synthesis (Sigma-Aldrich).

Besides the methods described here, the preparation of compounds of the formula (I) and salts thereof can take place completely or partially by solid-phase supported methods. For this purpose, individual intermediates or all intermediates in the synthesis or a synthesis adapted for the corresponding procedure are bonded to a synthesis resin. Solid-phase supported synthesis methods are sufficiently described in the specialist literature, e.g. Barry A. Bunin in “The Combinatorial Index”, Verlag Academic Press, 1998 and Combinatorial Chemistry—Synthesis, Analysis, Screening (editor Gunther Jung), Verlag Wiley, 1999. The use of solid-phase supported synthesis methods permits a series of protocols known in the literature, which again can be carried out manually or in an automated manner. The reactions can be carried out, for example, by means of IRORI technology in microreactors from Nexus Biosystems, 12140 Community Road, Poway, CA92064, USA.

Both on a solid phase and in liquid phase can the procedure of individual or several synthesis steps be supported through the use of microwave technology. The specialist literature describes a series of experimental protocols, for example in Microwaves in Organic and Medicinal Chemistry (editors C. O. Kappe and A. Stadler), Verlag Wiley, 2005.

The preparation according to the process described here produces compounds of the formula (I) and their salts in the form of substance collections which are called libraries. The present invention also provides libraries which comprise at least two compounds of the formula (I) and their salts.

The compounds of the formula (I) according to the invention (and/or their salts), hereinbelow also referred to together as “compounds according to the invention”, have excellent herbicidal efficacy against a broad spectrum of economically important monocotyledonous and dicotyledonous annual weed plants. The active compounds act efficiently even on perennial weeds which produce shoots from rhizomes, root stocks and other perennial organs and which are difficult to control.

The present invention therefore also relates to a method for controlling unwanted plants or for regulating the growth of plants, preferably in crops of plants, where one or more compound(s) according to the invention is/are applied to the plants (for example harmful plants such as monocotyledonous or dicotyledonous weeds or undesired crop plants), to the seeds (for example grains, seeds or vegetative propagules such as tubers or shoot parts with buds) or to the area on which the plants grow (for example the area under cultivation). In this context, the compounds according to the invention can be applied for example pre-sowing (if appropriate also by incorporation into the soil), pre-emergence or post-emergence. Specific examples may be mentioned of some representatives of the monocotyledonous and dicotyledonous weed flora which can be controlled by the compounds according to the invention, without the enumeration being restricted to certain species.

Monocotyledonous harmful plants of the genera: Aegilops, Agropyron, Agrostis, Alopecurus, Apera, Avena, Brachiaria, Bromus, Cenchrus, Commelina, Cynodon, Cyperus, Dactyloctenium, Digitaria, Echinochloa, Eleocharis, Eleusine, Eragrostis, Eriochloa, Festuca, Fimbristylis, Heteranthera, Imperata, Ischaemum, Leptochloa, Lolium, Monochoria, Panicum, Paspalum, Phalaris, Phleum, Poa, Rottboellia, Sagittaria, Scirpus, Setaria, Sorghum.

Dicotyledonous broad-leaved weeds of the genera: Abutilon, Amaranthus, Ambrosia, Anoda, Anthemis, Aphanes, Artemisia, Atriplex, Bellis, Bidens, Capsella, Carduus, Cassia, Centaurea, Chenopodium, Cirsium, Convolvulus, Datura, Desmodium, Emex, Erysimum, Euphorbia, Galeopsis, Galinsoga, Galium, Hibiscus, Ipomoea, Kochia, Lamium, Lepidium, Lindernia, Matricaria, Mentha, Mercurialis, Mullugo, Myosotis, Papaver, Pharbitis, Plantago, Polygonum, Portulaca, Ranunculus, Raphanus, Rorippa, Rotala, Rumex, Salsola, Senecio, Sesbania, Sida, Sinapis, Solanum, Sonchus, Sphenoclea, Stellaria, Taraxacum, Thlaspi, Trifolium, Urtica, Veronica, Viola, Xanthium.

If the compounds according to the invention are applied to the soil surface before germination, the weed seedlings are either prevented completely from emerging or else the weeds grow until they have reached the cotyledon stage, but then their growth stops, and, eventually, after three to four weeks have elapsed, they die completely.

If the active compounds are applied post-emergence to the green parts of the plants, growth stops after the treatment, and the harmful plants remain at the growth stage of the point of time of application, or they die completely after a certain time, so that in this manner competition by the weeds, which is harmful to the crop plants, is eliminated very early and in a sustained manner.

Although the compounds according to the invention display an outstanding herbicidal activity against monocotyledonous and dicotyledonous weeds, crop plants of economically important crops, for example dicotyledonous crops of the genera Arachis, Beta, Brassica, Cucumis, Cucurbita, Helianthus, Daucus, Glycine, Gossypium, Ipomoea, Lactuca, Linum, Lycopersicon, Nicotiana, Phaseolus, Pisum, Solanum, Vicia, or monocotyledonous crops of the genera Allium, Ananas, Asparagus, Avena, Hordeum, Oryza, Panicum, Saccharum, Secale, Sorghum, Triticale, Triticum, Zea, in particular Zea and Triticum, are damaged only to an insignificant extent, or not at all, depending on the structure of the respective compound according to the invention and its application rate. This is why the present compounds are highly suitable for the selective control of unwanted plant growth in plant crops such as agriculturally useful plants or ornamentals.

Moreover, the compounds according to the invention (depending on their respective structure and the application rate applied) have outstanding growth-regulatory properties in crop plants. They engage in the plant's metabolism in a regulatory fashion and can therefore be employed for the influencing, in a targeted manner, of plant constituents and for facilitating harvesting, such as, for example, by triggering desiccation and stunted growth. Moreover, they are also suitable for generally controlling and inhibiting unwanted vegetative growth without destroying the plants in the process. Inhibiting the vegetative growth plays an important role in many monocotyledonous and dicotyledonous crops since for example lodging can be reduced, or prevented completely, hereby.

By virtue of their herbicidal and plant-growth-regulatory properties, the active compounds can also be employed for controlling harmful plants in crops of genetically modified plants which are known or which are yet to be developed. In general, the transgenic plants are distinguished by especially advantageous properties, for example by resistances to certain pesticides, mainly certain herbicides, resistances to plant diseases or causative organisms of plant diseases, such as certain insects or microorganisms such as fungi, bacteria or viruses. Other specific characteristics relate, for example, to the harvested material with regard to quantity, quality, storability, composition and specific constituents. Thus, transgenic plants are known whose starch content is increased, or whose starch quality is altered, or those where the harvested material has a different fatty acid composition. Further particular characteristics may lie in tolerance or resistance to abiotic stressors, for example, heat, cold, drought, salt, and ultraviolet radiation.

It is preferred to use the compounds of the formula (I) according to the invention or their salts in economically important transgenic crops of useful plants and ornamentals, for example of cereals such as wheat, barley, rye, oats, millet, rice, cassaya and corn or else crops of sugar beet, cotton, soybean, oilseed rape, potato, tomato, peas and other vegetables.

It is possible with preference to employ the compounds of the formula (I) as herbicides in crops of useful plants which are resistant, or have been made resistant by recombinant means, to the phytotoxic effects of the herbicides.

Conventional methods of generating novel plants which have modified properties in comparison to plants occurring to date consist, for example, in traditional breeding methods and the generation of mutants. Alternatively, novel plants with altered properties can be generated with the aid of recombinant methods (see, for example, EP 0221044, EP 0131624). For example, the following have been described in several cases:

-   -   the modification, by recombinant technology, of crop plants with         the aim of modifying the starch synthesized in the plants (for         example WO 92/011376 A, WO 92/014827 A, WO 91/019806 A),     -   transgenic crop plants which are resistant to certain herbicides         of the glufosinate type (cf., for example, EP-A-0242236,         EP-A-0242246) or of the glyphosate type (WO 92/000377 A) or of         the sulfonylurea type (EP-A-0257993, U.S. Pat. No. 5,013,659),         or to combinations or mixtures of these herbicides which are         resistant as a result of ‘gene stacking’, such as transgenic         crop plants, e.g., corn or soybean, with the trade name or with         the designation Optimum™ GAT™ (glyphosate ALS tolerant).     -   transgenic crop plants, for example cotton, with the capability         of producing Bacillus thuringiensis toxins (Bt toxins), which         make the plants resistant to certain pests (EP-A-0142924,         EP-A-0193259),     -   transgenic crop plants with a modified fatty acid composition         (WO 91/013972 A),     -   genetically modified crop plants with novel constituents or         secondary metabolites, for example novel phytoalexins, which         bring about an increased disease resistance (EPA 0309862,         EPA0464461),     -   genetically modified plants with reduced photorespiration which         feature higher yields and higher stress tolerance (EPA 0305398),     -   transgenic crop plants which produce pharmaceutically or         diagnostically important proteins (“molecular pharming”),     -   transgenic crop plants which are distinguished by higher yields         or better quality,     -   transgenic crop plants which are distinguished by a combination,         for example, of the abovementioned novel properties (“gene         stacking”).

A large number of molecular-biological techniques by means of which novel transgenic plants with modified properties can be generated are known in principle; see, for example, I. Potrykus and G. Spangenberg (eds.) Gene Transfer to Plants, Springer Lab Manual (1995), Springer Verlag Berlin, Heidelberg. or Christou, “Trends in Plant Science” 1 (1996) 423-431.

To carry out such recombinant manipulations, nucleic acid molecules which allow mutagenesis or sequence changes by recombination of DNA sequences can be introduced into plasmids. For example, base substitutions can be carried out, part-sequences can be removed, or natural or synthetic sequences may be added with the aid of standard methods. To link the DNA fragments with one another, it is possible to add adapters or linkers to the fragments; see, for example, Sambrook et al., 1989, Molecular Cloning, A Laboratory Manual, 2nd ed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.; or Winnacker “Gene and Klone”, VCH Weinheim 2nd ed., 1996.

For example, the generation of plant cells with a reduced activity of a gene product can be achieved by expressing at least one corresponding antisense RNA, a sense RNA for achieving a cosuppression effect or by expressing at least one suitably constructed ribozyme which specifically cleaves transcripts of the abovementioned gene product.

To this end, it is possible to use DNA molecules which encompass the entire coding sequence of a gene product inclusive of any flanking sequences which may be present, and also DNA molecules which only encompass portions of the coding sequence, it being necessary for these portions to be long enough to have an antisense effect in the cells. The use of DNA sequences which have a high degree of homology to the coding sequences of a gene product, but are not completely identical to them, is also possible.

When expressing nucleic acid molecules in plants, the protein synthesized can be localized in any desired compartment of the plant cell. However, to achieve localization in a particular compartment, it is possible, for example, to link the coding region with DNA sequences which ensure localization in a particular compartment. Such sequences are known to those skilled in the art (see, for example, Braun et al., EMBO J. 11 (1992), 3219-3227; Wolter et al., Proc. Natl. Acad. Sci. USA 85 (1988), 846-850; Sonnewald et al., Plant J. 1 (1991), 95-106). The nucleic acid molecules can also be expressed in the organelles of the plant cells.

The transgenic plant cells can be regenerated by known techniques to give rise to entire plants. In principle, the transgenic plants can be plants of any desired plant species, i.e. not only monocotyledonous, but also dicotyledonous, plants.

Thus, transgenic plants can be obtained whose properties are altered by overexpression, suppression or inhibition of homologous (=natural) genes or gene sequences or the expression of heterologous (=foreign) genes or gene sequences.

It is preferred to employ the compounds (I) according to the invention in transgenic crops which are resistant to growth regulators such as, for example, 2,4 D dicamba, or to herbicides which inhibit essential plant enzymes, for example acetolactate synthases (ALS), EPSP synthases, glutamine synthases (GS) or hydroxyphenylpyruvate dioxygenases (HPPD), or to herbicides from the group of the sulfonylureas, the glyphosates, glufosinates or benzoylisoxazoles and analogous active compounds, or to any combinations of these active compounds.

With particular preference the compounds according to the invention can be used in transgenic crop plants which are resistant to a combination of glyphosates and glufosinates, glyphosates and sulfonylureas or imidazolinones. With very particular preference the compounds according to the invention can be used in transgenic crop plants such as, for example, corn or soybean with the tradename or the designation Optimum™ GAT™ (glyphosate ALS tolerant).

When the active compounds according to the invention are used in transgenic crops, effects are frequently observed—in addition to the effects on harmful plants which can be observed in other crops—which are specific for the application in the transgenic crop in question, for example a modified or specifically widened spectrum of weeds which can be controlled, modified application rates which may be employed for application, preferably good combinability with the herbicides to which the transgenic crop is resistant, and an effect on growth and yield of the transgenic crop plants.

The invention therefore also relates to the use of the compounds of the formula (I) according to the invention as herbicides for controlling harmful plants in transgenic crop plants.

The compounds according to the invention can be used in the form of wettable powders, emulsifiable concentrates, sprayable solutions, dusting products or granules in the customary formulations. The invention therefore also provides herbicidal and plant growth-regulating compositions which comprise the compounds according to the invention.

The compounds according to the invention can be formulated in various ways according to which biological and/or physicochemical parameters are mandated. Possible formulations include, for example: wettable powders (WP), water-soluble powders (SP), water-soluble concentrates, emulsifiable concentrates (EC), emulsions (EW) such as oil-in-water and water-in-oil emulsions, sprayable solutions, suspension concentrates (SC), oil- or water-based dispersions, oil-miscible solutions, capsule suspensions (CS), dusting products (DP), seed-dressing products, granules for scattering and soil application, granules (GR) in the form of microgranules, spray granules, coated granules and adsorption granules, water-dispersible granules (WG), water-soluble granules (SG), ULV formulations, microcapsules and waxes. These individual types of formulation are known in principle and are described, for example, in: Winnacker-Küchler, “Chemische Technologie” [Chemical technology], Volume 7, C. Hanser Verlag Munich, 4th Ed. 1986; Wade van Valkenburg, “Pesticide Formulations”, Marcel Dekker, N.Y., 1973; K. Martens, “Spray Drying” Handbook, 3rd Ed. 1979, G. Goodwin Ltd. London.

The necessary formulation assistants, such as inert materials, surfactants, solvents and further additives, are likewise known and are described, for example, in: Watkins, “Handbook of Insecticide Dust Diluents and Carriers”, 2nd Ed., Darland Books, Caldwell N.J.; H.v. Olphen, “Introduction to Clay Colloid Chemistry”; 2nd Ed., J. Wiley & Sons, N.Y.; C. Marsden, “Solvents Guide”; 2nd Ed., Interscience, N.Y. 1963; McCutcheon's “Detergents and Emulsifiers Annual”, MC Publ. Corp., Ridgewood N.J.; Sisley and Wood, “Encyclopedia of Surface Active Agents”, Chem. Publ. Co. Inc., N.Y. 1964; Schonfeldt, “Grenzflächenaktive Äthylenoxidaddukte” [Interface-active ethylene oxide adducts], Wiss. Verlagsgesell., Stuttgart 1976; Winnacker-Küchler, “Chemische Technologie”, Volume 7, C. Hanser Verlag Munich, 4th Ed. 1986.

Based on these formulations, it is also possible to produce combinations with other pesticidally active compounds, such as, for example, insecticides, acaricides, herbicides, fungicides, and also with safeners, fertilizers and/or growth regulators, for example in the form of a finished formulation or as a tank mix. Suitable safeners are, for example, mefenpyr-diethyl, cyprosulfamide, isoxadifen-ethyl, cloquintocet-mexyl and dichlormid.

Wettable powders are preparations which can be dispersed uniformly in water and, as well as the active compound, apart from a diluent or inert substance, also comprise surfactants of the ionic and/or nonionic type (wetting agents, dispersants), for example polyoxyethylated alkylphenols, polyoxyethylated fatty alcohols, polyoxyethylated fatty amines, fatty alcohol polyglycol ether sulfates, alkanesulfonates, alkylbenzenesulfonates, sodium lignosulfonate, sodium 2,2′-dinaphthylmethane-6,6′-disulfonate, sodium dibutylnaphthalenesulfonate or else sodium oleoylmethyltaurinate. To prepare the wettable powders, the herbicidally active compounds are ground finely, for example in customary apparatus such as hammer mills, blower mills and air-jet mills, and simultaneously or subsequently mixed with the formulation assistants.

Emulsifiable concentrates are prepared by dissolving the active compound in an organic solvent, for example butanol, cyclohexanone, dimethylformamide, xylene or else relatively high-boiling aromatics or hydrocarbons or mixtures of the organic solvents with addition of one or more surfactants of the ionic and/or nonionic type (emulsifiers). The emulsifiers used may, for example, be: calcium alkylarylsulfonate salts such as calcium dodecylbenzenesulfonate, or nonionic emulsifiers such as fatty acid polyglycol esters, alkylaryl polyglycol ethers, fatty alcohol polyglycol ethers, propylene oxide-ethylene oxide condensation products, alkyl polyethers, sorbitan esters, for example sorbitan fatty acid esters, or polyoxyethylene sorbitan esters, for example polyoxyethylene sorbitan fatty acid esters.

Dusts are obtained by grinding the active compound with finely distributed solid substances, for example talc, natural clays, such as kaolin, bentonite and pyrophyllite, or diatomaceous earth.

Suspension concentrates may be water- or oil-based. They may be prepared, for example, by wet grinding by means of commercial bead mills and optional addition of surfactants as have, for example, already been listed above for the other formulation types.

Emulsions, for example oil-in-water emulsions (EW), can be prepared, for example, by means of stirrers, colloid mills and/or static mixers using aqueous organic solvents and optionally surfactants, as have, for example, already been listed above for the other formulation types.

Granules can be prepared either by spraying the active compound onto granular inert material capable of adsorption or by applying active compound concentrates to the surface of carrier substances, such as sand, kaolinites or granular inert material, by means of adhesives, for example polyvinyl alcohol, sodium polyacrylate or mineral oils. Suitable active compounds can also be granulated in the manner customary for the preparation of fertilizer granules—if desired as a mixture with fertilizers.

Water-dispersible granules are prepared generally by the customary processes such as spray-drying, fluidized bed granulation, pan granulation, mixing with high-speed mixers and extrusion without solid inert material.

For the preparation of pan, fluidized bed, extruder and spray granules, see, for example, processes in “Spray-Drying Handbook” 3rd ed. 1979, G. Goodwin Ltd., London; J. E. Browning, “Agglomeration”, Chemical and Engineering 1967, pages 147 ff; “Perry's Chemical Engineer's Handbook”, 5th Ed McGraw-Hill, New York 1973, p. 8-57.

For further details regarding the formulation of crop protection compositions, see, for example, G. C. Klingman, “Weed Control as a Science”, John Wiley and Sons, Inc., New York, 1961, pages 81-96 and J. D. Freyer, S. A. Evans, “Weed Control Handbook”, 5th Ed., Blackwell Scientific Publications, Oxford, 1968, pages 101-103.

The agrochemical formulations contain generally from 0.1 to 99% by weight, in particular from 0.1 to 95% by weight, of compounds according to the invention.

In wettable powders, the active compound concentration is, for example, from about 10 to 90% by weight, the remainder to 100% by weight consisting of customary formulation components. In the case of emulsifiable concentrates, the active compound concentration can be from about 1 to 90, preferably from 5 to 80, % by weight. Formulations in the form of dusts comprise from 1 to 30% by weight of active compound, preferably usually from 5 to 20% by weight of active compound; sprayable solutions contain from about 0.05 to 80% by weight, preferably from 2 to 50% by weight of active compound. In the case of water-dispersible granules, the active compound content depends partially on whether the active compound is present in liquid or solid form and on which granulation auxiliaries, fillers, etc., are used. In the water-dispersible granules, the content of active compound is, for example, between 1 and 95% by weight, preferably between 10 and 80% by weight.

In addition, the active compound formulations mentioned optionally comprise the respective customary adhesives, wetting agents, dispersants, emulsifiers, penetrants, preservatives, antifreeze agents and solvents, fillers, carriers and dyes, defoamers, evaporation inhibitors and agents which influence the pH and the viscosity.

Based on these formulations, it is also possible to produce combinations with other pesticidally active compounds, such as, for example, insecticides, acaricides, herbicides, fungicides, and also with safeners, fertilizers and/or growth regulators, for example in the form of a finished formulation or as a tank mix.

Active compounds which can be employed in combination with the compounds according to the invention in mixed formulations or in the tank mix are, for example, known active compounds which are based on the inhibition of, for example, acetolactate synthase, acetyl-CoA carboxylase, cellulose synthase, enolpyruvylshikimate-3-phosphate synthase, glutamine synthetase, p-hydroxyphenylpyruvate dioxygenase, phytoen desaturase, photosystem I, photosystem II, protoporphyrinogen oxidase, as are described in, for example, Weed Research 26 (1986) 441-445 or “The Pesticide Manual”, 15th edition, The British Crop Protection Council and the Royal Soc. of Chemistry, 2003 and the literature cited therein. Known herbicides or plant growth regulators which can be combined with the compounds according to the invention are, for example, the following active compounds (the compounds are either designated by the common name according to the International Organization for Standardization (ISO) or by the chemical name, or by the code number) and always comprise all use forms such as acids, salts, esters and isomers such as stereoisomers and optical isomers. Here, by way of example, one and in some cases a plurality of use forms are mentioned: acetochlor, acibenzolar, acibenzolar-S-methyl, acifluorfen, acifluorfen-sodium, aclonifen, alachlor, allidochlor, alloxydim, alloxydim-sodium, ametryn, amicarbazone, amidochlor, amidosulfuron, aminocyclopyrachlor, aminopyralid, amitrole, ammonium sulfamate, ancymidol, anilofos, asulam, atrazine, azafenidin, azimsulfuron, aziprotryn, beflubutamid, benazolin, benazolin-ethyl, bencarbazone, benfluralin, benfuresate, bensulide, bensulfuron, bensulfuron-methyl, bentazone, benzfendizone, benzobicyclon, benzofenap, benzofluor, benzoylprop, bicyclopyrone, bifenox, bilanafos, bilanafos-sodium, bispyribac, bispyribac-sodium, bromacil, bromobutide, bromofenoxim, bromoxynil, bromuron, buminafos, busoxinone, butachlor, butafenacil, butamifos, butenachlor, butralin, butroxydim, butylate, cafenstrole, carbetamide, carfentrazone, carfentrazone-ethyl, chlomethoxyfen, chloramben, chlorazifop, chlorazifop-butyl, chlorbromuron, chlorbufam, chlorfenac, chlorfenac-sodium, chlorfenprop, chlorflurenol, chlorflurenol-methyl, chloridazon, chlorimuron, chlorimuron-ethyl, chlormequat chloride, chlornitrofen, chlorophthalim, chlorthal-dimethyl, chlorotoluron, chlorsulfuron, cinidon, cinidon-ethyl, cinmethylin, cinosulfuron, clethodim, clodinafop, clodinafop-propargyl, clofencet, clomazone, clomeprop, cloprop, clopyralid, cloransulam, cloransulam-methyl, cumyluron, cyanamide, cyanazine, cyclanilide, cycloate, cyclosulfamuron, cycloxydim, cycluron, cyhalofop, cyhalofop-butyl, cyperquat, cyprazine, cyprazole, 2,4-D, 2,4-DB, daimuron/dymron, dalapon, daminozide, dazomet, n-decanol, desmedipham, desmetryn, detosyl pyrazolate (DTP), diallate, dicamba, dichlobenil, dichlorprop, dichlorprop-P, diclofop, diclofop-methyl, diclofop-P-methyl, diclosulam, diethatyl, diethatyl-ethyl, difenoxuron, difenzoquat, diflufenican, diflufenzopyr, diflufenzopyr-sodium, dimefuron, dikegulac-sodium, dimefuron, dimepiperate, dimethachlor, dimethametryn, dimethenamid, dimethenamid-P, dimethipin, dimetrasulfuron, dinitramine, dinoseb, dinoterb, diphenamid, dipropetryn, diquat, diquat dibromide, dithiopyr, diuron, DNOC, eglinazine-ethyl, endothal, EPTC, esprocarb, ethalfluralin, ethametsulfuron, ethametsulfuron-methyl, ethephon, ethidimuron, ethiozin, ethofumesate, ethoxyfen, ethoxyfen-ethyl, ethoxysulfuron, etobenzanid, F-5331, i.e. N-[2-chloro-4-fluoro-5-[4-(3-fluoropropyl)-4,5-dihydro-5-oxo-1H-tetrazol-1-yl]-phenyl]-ethanesulfonamide, F-7967, i.e., 3-[7-chloro-5-fluoro-2-(trifluoromethyl)-1H-benzimidazol-4-yl]-1-methyl-6-(trifluoromethyl)pyrimidine-2,4(1H, 3H)-dione, fenoprop, fenoxaprop, fenoxaprop-P, fenoxaprop-ethyl, fenoxaprop-P-ethyl, fenoxasulfone, fentrazamide, fenuron, flamprop, flamprop-M-isopropyl, flamprop-M-methyl, flazasulfuron, florasulam, fluazifop, fluazifop-P, fluazifop-butyl, fluazifop-P-butyl, fluazolate, flucarbazone, flucarbazone-sodium, flucetosulfuron, fluchloralin, flufenacet (thiafluamide), flufenpyr, flufenpyr-ethyl, flumetralin, flumetsulam, flumiclorac, flumiclorac-pentyl, flumioxazin, flumipropyn, fluometuron, fluorodifen, fluoroglycofen, fluoroglycofen-ethyl, flupoxam, flupropacil, flupropanate, flupyrsulfuron, flupyrsulfuron-methyl-sodium, flurenol, flurenol-butyl, fluridone, fluorochloridone, fluoroxypyr, fluoroxypyr-meptyl, flurprimidol, flurtamone, fluthiacet, fluthiacet-methyl, fluthiamide, fomesafen, foramsulfuron, forchlorfenuron, fosamine, furyloxyfen, gibberellic acid, glufosinate, glufosinate-ammonium, glufosinate-P, glufosinate-P-ammonium, glufosinate-P-sodium, glyphosate, glyphosate-isopropylammonium, H-9201, i.e., O-(2,4-dimethyl-6-nitrophenyl)-O-ethyl-isopropylphosphoramidothioate, halosafen, halosulfuron, halosulfuron-methyl, haloxyfop, haloxyfop-P, haloxyfop-ethoxyethyl, haloxyfop-P-ethoxyethyl, haloxyfop-methyl, haloxyfop-P-methyl, hexazinone, HW-02, i.e., 1-(dimethoxyphosphoryl)-ethyl(2,4-dichlorophenoxy)acetate, imazamethabenz, imazamethabenz-methyl, imazamox, imazamox-ammonium, imazapic, imazapyr, imazapyr-isopropylammonium, imazaquin, imazaquin-ammonium, imazethapyr, imazethapyr-ammonium, imazosulfuron, inabenfide, indanofan, indaziflam, indoleacetic acid (IAA), 4-indol-3-ylbutyric acid (IBA), iodosulfuron, iodosulfuron-methyl-sodium, ioxynil, ipfencarbazone, isocarbamid, isopropalin, isoproturon, isouron, isoxaben, isoxachlortole, isoxaflutole, isoxapyrifop, KUH-043, i.e., 3-({[5-(difluoromethyl)-1-methyl-3-(trifluoromethyl)-1H-pyrazol-4-yl]methyl}sulfonyl)-5,5-dimethyl-4,5-dihydro-1,2-oxazole, karbutilate, ketospiradox, lactofen, lenacil, linuron, maleic hydrazide, MCPA, MCPB, MCPB-methyl, -ethyl and -sodium, mecoprop, mecoprop-sodium, mecoprop-butotyl, mecoprop-P-butotyl, mecoprop-P-dimethylammonium, mecoprop-P-2-ethylhexyl, mecoprop-P-potassium, mefenacet, mefluidide, mepiquat-chloride, mesosulfuron, mesosulfuron-methyl, mesotrione, methabenzthiazuron, metam, metamifop, metamitron, metazachlor, metazasulfuron, methazole, methiopyrsulfuron, methiozolin, methoxyphenone, methyldymron, 1-methylcyclopropene, methylisothiocyanate, metobenzuron, metobromuron, metolachlor, S-metolachlor, metosulam, metoxuron, metribuzin, metsulfuron, metsulfuron-methyl, molinate, monalide, monocarbamide, monocarbamide dihydrogensulfate, monolinuron, monosulfuron, monosulfuron-ester, monuron, MT 128, i.e., 6-chloro-N-[(2E)-3-chloroprop-2-en-1-yl]-5-methyl-N-phenylpyridazin-3-amine, MT-5950, i.e. N-[3-chloro-4-(1-methylethyl)-phenyl]-2-methylpentanamide, NGGC-011, naproanilide, napropamide, naptalam, NC-310, i.e. 4-(2,4-dichlorobenzoyl)-1-methyl-5-benzyloxypyrazole, neburon, nicosulfuron, nipyraclofen, nitralin, nitrofen, nitrophenolate sodium (isomer mixture), nitrofluorfen, nonanoic acid, norflurazon, orbencarb, orthosulfamuron, oryzalin, oxadiargyl, oxadiazon, oxasulfuron, oxaziclomefone, oxyfluorfen, paclobutrazol, paraquat, paraquat-dichlorid, pelargonic acid (nonanoic acid), pendimethalin, pendralin, penoxsulam, pentanochlor, pentoxazone, perfluidone, pethoxamid, phenisopham, phenmedipham, phenmedipham-ethyl, picloram, picolinafen, pinoxaden, piperophos, pirifenop, pirifenop-butyl, pretilachlor, primisulfuron, primisulfuron-methyl, probenazole, profluazol, procyazine, prodiamine, prifluraline, profoxydim, prohexadione, prohexadione-calcium, prohydrojasmone, prometon, prometryn, propachlor, propanil, propaquizafop, propazine, propham, propisochlor, propoxycarbazone, propoxycarbazone-sodium, propyrisulfuron, propyzamide, prosulfalin, prosulfocarb, prosulfuron, prynachlor, pyraclonil, pyraflufen, pyraflufen-ethyl, pyrasulfotole, pyrazolynate (pyrazolate), pyrazosulfuron, pyrazosulfuron-ethyl, pyrazoxyfen, pyribambenz, pyribambenz-isopropyl, pyribambenz-propyl, pyribenzoxim, pyributicarb, pyridafol, pyridate, pyriftalid, pyriminobac, pyriminobac-methyl, pyrimisulfan, pyrithiobac, pyrithiobac-sodium, pyroxasulfone, pyroxsulam, quinclorac, quinmerac, quinoclamine, quizalofop, quizalofop-ethyl, quizalofop-P, quizalofop-P-ethyl, quizalofop-P-tefuryl, rimsulfuron, saflufenacil, secbumeton, sethoxydim, siduron, simazine, simetryn, SN-106279, i.e. methyl-(2R)-2({7-[2-chloro-4-(trifluoromethyl)phenoxy]-2-naphthyl}oxy)propanoate, sulcotrione, sulfallate (CDEC), sulfentrazone, sulfometuron, sulfometuron-methyl, sulfosate (glyphosate-trimesium), sulfosulfuron, SYN-523, SYP-249, i.e., 1-ethoxy-3-methyl-1-oxobut-3-en-2-yl-5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoate, SYP-300, i.e., 1-[7-fluoro-3-oxo-4-(prop-2-yn-1-yl)-3,4-dihydro-2H-1,4-benzoxazin-6-yl]-3-propyl-2-thioxoimidazolidine-4,5-dione, tebutam, tebuthiuron, tecnazene, tefuryltrione, tembotrione, tepraloxydim, terbacil, terbucarb, terbuchlor, terbumeton, terbuthylazine, terbutryn, thenylchlor, thiafluamide, thiazafluoron, thiazopyr, thidiazimin, thidiazuron, thiencarbazone, thiencarbazone-methyl, thifensulfuron, thifensulfuron-methyl, thiobencarb, tiocarbazil, topramezone, tralkoxydim, triallate, triasulfuron, triaziflam, triazofenamide, tribenuron, tribenuron-methyl, trichloroacetic acid (TCA), triclopyr, tridiphane, trietazine, trifloxysulfuron, trifloxysulfuron-sodium, trifluralin, triflusulfuron, triflusulfuron-methyl, trimeturon, trinexapac, trinexapac-ethyl, tritosulfuron, tsitodef, uniconazole, uniconazole-P, vernolate, ZJ-0862 i.e. 3,4-dichloro-N-{2-[(4,6-dimethoxypyrimidin-2-yl)oxy]benzyl}aniline, and also the following compounds:

For application, the formulations present in commercial form are, if appropriate, diluted in a customary manner, for example, in the case of wettable powders, emulsifiable concentrates, dispersions and water-dispersible granules, with water. Preparations in the form of dusts, granules for soil application or granules for broadcasting and sprayable solutions are usually not diluted further with other inert substances prior to application.

The required application rate of the compounds of the formula (I) varies according to the external conditions such as, inter alia, temperature, humidity and the type of herbicide used. It may vary within wide limits, for example between 0.001 and 1.0 kg/ha or more of active substance; however, preferably it is between 0.005 and 750 g/ha.

The examples which follow illustrate the invention.

A. Chemical Examples Preparation of 5-hydroxy-1,3-dimethyl-4-(2-methyl-3-methylthio-4-pentafluoroethyl-benzoyl)pyrazole (tabular example No. 3-145) Step 1: Synthesis of 3-fluoro-4-(pentafluoroethyl)bromobenzene

13.2 g (91.9 mmol) of copper(I) bromide were cooled to −5° C. in 80 ml of dry N,N-dimethylformamide. Under nitrogen, 14.7 g (76.7 mmol) of trimethyl-(pentafluoroethyl)silane were added. 4.45 g (76.7 mmol) of potassium fluoride (spray-dried) were added in portions over the course of 30 minutes at a rate such that the internal temperature remained below 0° C. The mixture was stirred at 0° C. for 1 hour and was then warmed to 20° C. over the course of 12 hours. Thereafter 10 ml of dry 1,3-dimethyl-2-imidazolidinone and 22 g (73.1 mmol) of 3-fluoro-4-iodo-bromobenzene were added. The contents were stirred at 75° C. for 14 hours. Then all of the volatile constituents were distilled off to dryness, the distillate being collected in a cold trap cooled with liquid nitrogen. The distillate was subsequently warmed to 20° C. and dissolved in 500 ml of diethyl ether. This solution was washed with four times 100 ml of water and then with two times 100 ml of saturated aqueous NaCl solution. The organic phase was then dried, and the solvent was removed on a Vigreux column. Subsequent distillation of the residue on a Vigreux column gave 16.1 g of product (boiling point: 86-87° C. (75 mmHg)) with a purity of 99% by weight.

Step 2: Synthesis of 3-fluoro-4-(pentafluoroethyl)benzoic acid

A solution of 16.0 g (99% by weight; 54.1 mmol) of 3-fluoro-4-(pentafluoroethyl)-bromobenzene in 110 ml of THF was cooled to −10° C. Added dropwise over the course of 30 minutes were 36.8 ml of a 2M (73.6 mmol) solution of isopropyl-magnesium chloride. The mixture was stirred at −10° C. for 2.5 hours and then cautiously poured onto an excess of dry ice. For working up, 130 ml of water were added, and the mixture was subsequently extracted once with 10 ml of diethyl ether. The aqueous phase was acidified with half-concentrated hydrochloric acid and then extracted with four times 150 ml of diethyl ether. The combined organic phases were dried and the filtrate was freed from the solvent. The residue was recrystallized from CHCl₃, giving 10.7 g of product with a purity of 98% by weight.

Step 3: Synthesis of 3-fluor-2-methyl-4-(pentafluoroethyl)benzoic acid

5.00 g (98% by weight; 19.0 mmol) of 3-fluoro-4-(pentafluoroethyl)benzoic acid were introduced into 40 ml of dry tetrahydrofuran. 4.73 g (40.7 mmol) of 1,2-bis-(dimethylamino)ethane were added, and the mixture was then cooled to −40° C. Then 16.3 ml of a 2.5 M solution (40.7 mmol) of n-butyllithium in hexane were added dropwise at a rate such that the temperature was in a range from −33° C. to −35° C. The contents were stirred at −35° C. for 4 hours. Then a solution of 8.25 g (58.1 mmol) of iodomethane in 10 ml of dry THF was added dropwise, and the mixture was stirred at −35° C. for 1 hour. Thereafter the contents were warmed to room temperature (RT) and stirred at this temperature for 16 hours. For working up, 50 ml of 2M hydrochloric acid were cautiously added, and then the aqueous phase was extracted with diethyl ether. The combined organic phases were dried and freed from the solvents. The residue was stirred in n-heptane and subsequently filtered. This gave 2.33 g of residue as a clean product. The filtrate was freed from the solvent, and the residue was again stirred in n-heptane. Filtration produced 590 mg of residue, which was identified as a product with a purity of 70% by weight.

Step 4: Synthesis of methyl 3-fluoro-2-methyl-4-(pentafluoroethyl)benzoate

2.33 g (8.56 mmol) of 3-fluoro-2-methyl-4-(pentafluoroethyl)benzoic acid were introduced into 30 ml of methanol and admixed with 2 ml of concentrated sulfuric acid. The mixture was subsequently heated at reflux until a check by HPLC indicated full conversion. The contents were freed from the solvent, and the residue was taken up in water. The mixture was extracted twice with ethyl acetate, and the combined organic phases were washed once with saturated aqueous sodium hydrogen-carbonate solution. The organic phase was dried and freed from the solvent. The residue obtained was 2.1 g of clean product.

Step 5: Synthesis of methyl 2-methyl-3-(methylthio)-4-(pentafluoroethyl)benzoate

2.1 g (7.34 mmol) of methyl 3-fluoro-2-methyl-4-(pentafluoroethyl)benzoate were introduced into 20 ml of N,N-dimethylformamide and then admixed with 758 mg (95% by weight; 10.3 mmol) of sodium thiomethoxide. The mixture was stirred at RT for 2 hours and then freed from the solvent. The residue was taken up in ethyl acetate and water, the aqueous phase was extracted twice with ethyl acetate, and, finally, the combined organic phases were dried and freed from the solvent. The residue was purified by chromatography, giving 1.28 g of clean product.

Step 6: Synthesis of 2-methyl-3-(methylthio)-4-(pentafluoroethyl)benzoic acid (No. 5-145)

530 mg (1.69 mmol) of methyl 2-methyl-3-(methylthio)-4-(pentafluoroethyl)benzoate were introduced into 10 ml of methanol and admixed with 0.5 ml of 20% strength aqueous sodium hydroxide solution. The contents were stirred at room temperature until a check on the reaction by thin-layer chromatography indicated complete conversion. The mixture was freed from the solvent, and the residue was taken up in a little water. The mixture was acidified with 1M hydrochloric acid, then stirred for 5 minutes and finally filtered. The residue obtained was 470 mg of clean product.

Step 7: Synthesis of 1,3-dimethyl-5-(2″-methyl-3″-(methylthio)-4″-(pentafluoroethyl)benzoyloxy)pyrazole

360 mg (1.20 mmol) of 2-methyl-3-(methylthio)-4-(pentafluoroethyl)benzoic acid were introduced into 20 ml of dry dichloromethane and admixed in succession with 198 mg (1.56 mmol) of oxalyl dichloride and also with two drops of N,N-dimethyl-formamide. After the end of evolution of gas, the mixture was heated under reflux for 10 minutes. When a check on the reaction by thin-layer chromatography had indicated complete conversion, the contents were freed from the solvent, and the residue was then taken up in 20 ml of dry dichloromethane. The mixture was admixed with 161 mg (1.44 mmol) of 5-hydroxy-1,3-dimethylpyrazole, and then 243 mg (2.40 mmol) of triethylamine were added dropwise. The contents were stirred at RT for 16 hours. For working up, 3 ml of 1M hydrochloric acid were added, and, following phase separation, the organic phase was freed from the solvent. The residue, finally, was purified by chromatography, giving 410 mg of clean product.

Step 8: Synthesis of 5-hydroxy-1,3-dimethyl-4-(2′-methyl-3′-(methylthio)-4′-(pentafluoroethyl)benzoyl)pyrazole (No. 3-145)

136 mg (0.345 mmol) of 1,3-dimethyl-5-(2′-methyl-3′-(methylthio)-4′-(pentafluoro-ethyl)benzoyloxy)pyrazole were introduced into 15 ml of acetonitrile and admixed in succession with 70 mg (0.69 mmol) of triethylamine and also with eight drops of trimethylsilyl cyanide. The mixture was stirred at RT for 16 hours. For working up, the contents were freed from the solvent, and the residue was taken up in 15 ml of dichloromethane. 3 ml of 1M hydrochloric acid were added, and, following phase separation, the organic phase was freed from the solvent. The residue was purified by chromatography, giving 71.3 mg of product with a purity of 95% by weight.

The examples listed in tables below were prepared in analogy to methods identified above or are obtainable in analogy to methods identified above. These compounds are very particularly preferred.

The abbreviations used have the following meanings:

Bu = butyl Et = ethyl Me = methyl Pr = propyl i = iso s = secondary t = tertiary Ph = phenyl

TABLE 1 Inventive compounds of the formula (I) in which R² is methyl, and R³ and R⁴ are each hydrogen

No. X R¹ n Y Physical data: ¹H-NMR: δ [CDCl₃] 1-1 Me Me 0 CF₂Cl 1-2 Me Et 0 CF₂Cl 1-3 Me n-Pr 0 CF₂Cl 1-4 Me i-Pr 0 CF₂Cl 1-5 Me n-Bu 0 CF₂Cl 1-6 Me i-Bu 0 CF₂Cl 1-7 Me s-Bu 0 CF₂Cl 1-8 Me t-Bu 0 CF₂Cl 1-9 Me Me 1 CF₂Cl 1-10 Me Et 1 CF₂Cl 1-11 Me n-Pr 1 CF₂Cl 1-12 Me i-Pr 1 CF₂Cl 1-13 Me n-Bu 1 CF₂Cl 1-14 Me i-Bu 1 CF₂Cl 1-15 Me s-Bu 1 CF₂Cl 1-16 Me t-Bu 1 CF₂Cl 1-17 Me Me 2 CF₂Cl 1-18 Me Et 2 CF₂Cl 1-19 Me n-Pr 2 CF₂Cl 1-20 Me i-Pr 2 CF₂Cl 1-21 Me n-Bu 2 CF₂Cl 1-22 Me i-Bu 2 CF₂Cl 1-23 Me s-Bu 2 CF₂Cl 1-24 Me t-Bu 2 CF₂Cl 1-25 Et Me 0 CF₂Cl 1-26 Et Et 0 CF₂Cl 1-27 Et n-Pr 0 CF₂Cl 1-28 Et i-Pr 0 CF₂Cl 1-29 Et n-Bu 0 CF₂Cl 1-30 Et i-Bu 0 CF₂Cl 1-31 Et s-Bu 0 CF₂Cl 1-32 Et t-Bu 0 CF₂Cl 1-33 Et Me 1 CF₂Cl 1-34 Et Et 1 CF₂Cl 1-35 Et n-Pr 1 CF₂Cl 1-36 Et i-Pr 1 CF₂Cl 1-37 Et n-Bu 1 CF₂Cl 1-38 Et i-Bu 1 CF₂Cl 1-39 Et s-Bu 1 CF₂Cl 1-40 Et t-Bu 1 CF₂Cl 1-41 Et Me 2 CF₂Cl 1-42 Et Et 2 CF₂Cl 1-43 Et n-Pr 2 CF₂Cl 1-44 Et i-Pr 2 CF₂Cl 1-45 Et n-Bu 2 CF₂Cl 1-46 Et i-Bu 2 CF₂Cl 1-47 Et s-Bu 2 CF₂Cl 1-48 Et t-Bu 2 CF₂Cl 1-49 Me Me 0 CFCl₂ 1-50 Me Et 0 CFCl₂ 1-51 Me n-Pr 0 CFCl₂ 1-52 Me i-Pr 0 CFCl₂ 1-53 Me n-Bu 0 CFCl₂ 1-54 Me i-Bu 0 CFCl₂ 1-55 Me s-Bu 0 CFCl₂ 1-56 Me t-Bu 0 CFCl₂ 1-57 Me Me 1 CFCl₂ 1-58 Me Et 1 CFCl₂ 1-59 Me n-Pr 1 CFCl₂ 1-60 Me i-Pr 1 CFCl₂ 1-61 Me n-Bu 1 CFCl₂ 1-62 Me i-Bu 1 CFCl₂ 1-63 Me s-Bu 1 CFCl₂ 1-64 Me t-Bu 1 CFCl₂ 1-65 Me Me 2 CFCl₂ 1-66 Me Et 2 CFCl₂ 1-67 Me n-Pr 2 CFCl₂ 1-68 Me i-Pr 2 CFCl₂ 1-69 Me n-Bu 2 CFCl₂ 1-70 Me i-Bu 2 CFCl₂ 1-71 Me s-Bu 2 CFCl₂ 1-72 Me t-Bu 2 CFCl₂ 1-73 Et Me 0 CFCl₂ 1-74 Et Et 0 CFCl₂ 1-75 Et n-Pr 0 CFCl₂ 1-76 Et i-Pr 0 CFCl₂ 1-77 Et n-Bu 0 CFCl₂ 1-78 Et i-Bu 0 CFCl₂ 1-79 Et s-Bu 0 CFCl₂ 1-80 Et t-Bu 0 CFCl₂ 1-81 Et Me 1 CFCl₂ 1-82 Et Et 1 CFCl₂ 1-83 Et n-Pr 1 CFCl₂ 1-84 Et i-Pr 1 CFCl₂ 1-85 Et n-Bu 1 CFCl₂ 1-86 Et i-Bu 1 CFCl₂ 1-87 Et s-Bu 1 CFCl₂ 1-88 Et t-Bu 1 CFCl₂ 1-89 Et Me 2 CFCl₂ 1-90 Et Et 2 CFCl₂ 1-91 Et n-Pr 2 CFCl₂ 1-92 Et i-Pr 2 CFCl₂ 1-93 Et n-Bu 2 CFCl₂ 1-94 Et i-Bu 2 CFCl₂ 1-95 Et s-Bu 2 CFCl₂ 1-96 Et t-Bu 2 CFCl₂ 1-97 Me Me 0 CCl₃ 1-98 Me Et 0 CCl₃ 1-99 Me n-Pr 0 CCl₃ 1-100 Me i-Pr 0 CCl₃ 1-101 Me n-Bu 0 CCl₃ 1-102 Me i-Bu 0 CCl₃ 1-103 Me s-Bu 0 CCl₃ 1-104 Me t-Bu 0 CCl₃ 1-105 Me Me 1 CCl₃ 1-106 Me Et 1 CCl₃ 1-107 Me n-Pr 1 CCl₃ 1-108 Me i-Pr 1 CCl₃ 1-109 Me n-Bu 1 CCl₃ 1-110 Me i-Bu 1 CCl₃ 1-111 Me s-Bu 1 CCl₃ 1-112 Me t-Bu 1 CCl₃ 1-113 Me Me 2 CCl₃ 1-114 Me Et 2 CCl₃ 1-115 Me n-Pr 2 CCl₃ 1-116 Me i-Pr 2 CCl₃ 1-117 Me n-Bu 2 CCl₃ 1-118 Me i-Bu 2 CCl₃ 1-119 Me s-Bu 2 CCl₃ 1-120 Me t-Bu 2 CCl₃ 1-121 Et Me 0 CCl₃ 1-122 Et Et 0 CCl₃ 1-123 Et n-Pr 0 CCl₃ 1-124 Et i-Pr 0 CCl₃ 1-125 Et n-Bu 0 CCl₃ 1-126 Et i-Bu 0 CCl₃ 1-127 Et s-Bu 0 CCl₃ 1-128 Et t-Bu 0 CCl₃ 1-129 Et Me 1 CCl₃ 1-130 Et Et 1 CCl₃ 1-131 Et n-Pr 1 CCl₃ 1-132 Et i-Pr 1 CCl₃ 1-133 Et n-Bu 1 CCl₃ 1-134 Et i-Bu 1 CCl₃ 1-135 Et s-Bu 1 CCl₃ 1-136 Et t-Bu 1 CCl₃ 1-137 Et Me 2 CCl₃ 1-138 Et Et 2 CCl₃ 1-139 Et n-Pr 2 CCl₃ 1-140 Et i-Pr 2 CCl₃ 1-141 Et n-Bu 2 CCl₃ 1-142 Et i-Bu 2 CCl₃ 1-143 Et s-Bu 2 CCl₃ 1-144 Et t-Bu 2 CCl₃ 1-145 Me Me 0 C₂F₅ 7.61 (d, 1H), 7.47 (d, 1H), 7.31 (s, 1H), 3.72 (s, 3H), 2.69 (s, 3H), 2.30 (s, 3H) 1-146 Me Et 0 C₂F₅ 1-147 Me n-Pr 0 C₂F₅ 1-148 Me i-Pr 0 C₂F₅ 1-149 Me n-Bu 0 C₂F₅ 1-150 Me i-Bu 0 C₂F₅ 1-151 Me s-Bu 0 C₂F₅ 1-152 Me t-Bu 0 C₂F₅ 1-153 Me Me 1 C₂F₅ 7.63 (d, 1H), 7.57 (d, 1H), 7.33 (s, 1H), 3.73 (s, 3H), 3.07 (s, 3H), 2.91 (s, 3H) 1-154 Me Et 1 C₂F₅ 1-155 Me n-Pr 1 C₂F₅ 1-156 Me i-Pr 1 C₂F₅ 1-157 Me n-Bu 1 C₂F₅ 1-158 Me i-Bu 1 C₂F₅ 1-159 Me s-Bu 1 C₂F₅ 1-160 Me t-Bu 1 C₂F₅ 1-161 Me Me 2 C₂F₅ 7.76 (d, 1H), 7.64 (d, 1H), 7.30 (s, 1H), 3.73 (s, 3H), 3.29 (s, 3H), 2.77 (s, 3H) 1-162 Me Et 2 C₂F₅ 1-163 Me n-Pr 2 C₂F₅ 1-164 Me i-Pr 2 C₂F₅ 1-165 Me n-Bu 2 C₂F₅ 1-166 Me i-Bu 2 C₂F₅ 1-167 Me s-Bu 2 C₂F₅ 1-168 Me t-Bu 2 C₂F₅ 1-169 Et Me 0 C₂F₅ 1-170 Et Et 0 C₂F₅ 1-171 Et n-Pr 0 C₂F₅ 1-172 Et i-Pr 0 C₂F₅ 1-173 Et n-Bu 0 C₂F₅ 1-174 Et i-Bu 0 C₂F₅ 1-175 Et s-Bu 0 C₂F₅ 1-176 Et t-Bu 0 C₂F₅ 1-177 Et Me 1 C₂F₅ 1-178 Et Et 1 C₂F₅ 1-179 Et n-Pr 1 C₂F₅ 1-180 Et i-Pr 1 C₂F₅ 1-181 Et n-Bu 1 C₂F₅ 1-182 Et i-Bu 1 C₂F₅ 1-183 Et s-Bu 1 C₂F₅ 1-184 Et t-Bu 1 C₂F₅ 1-185 Et Me 2 C₂F₅ 1-186 Et Et 2 C₂F₅ 1-187 Et n-Pr 2 C₂F₅ 1-188 Et i-Pr 2 C₂F₅ 1-189 Et n-Bu 2 C₂F₅ 1-190 Et i-Bu 2 C₂F₅ 1-191 Et s-Bu 2 C₂F₅ 1-192 Et t-Bu 2 C₂F₅ 1-193 Me Me 0 CF(CF₃)₂ 1-194 Me Et 0 CF(CF₃)₂ 1-195 Me n-Pr 0 CF(CF₃)₂ 1-196 Me i-Pr 0 CF(CF₃)₂ 1-197 Me n-Bu 0 CF(CF₃)₂ 1-198 Me i-Bu 0 CF(CF₃)₂ 1-199 Me s-Bu 0 CF(CF₃)₂ 1-200 Me t-Bu 0 CF(CF₃)₂ 1-201 Me Me 1 CF(CF₃)₂ 1-202 Me Et 1 CF(CF₃)₂ 1-203 Me n-Pr 1 CF(CF₃)₂ 1-204 Me i-Pr 1 CF(CF₃)₂ 1-205 Me n-Bu 1 CF(CF₃)₂ 1-206 Me i-Bu 1 CF(CF₃)₂ 1-207 Me s-Bu 1 CF(CF₃)₂ 1-208 Me t-Bu 1 CF(CF₃)₂ 1-209 Me Me 2 CF(CF₃)₂ 1-210 Me Et 2 CF(CF₃)₂ 1-211 Me n-Pr 2 CF(CF₃)₂ 1-212 Me i-Pr 2 CF(CF₃)₂ 1-213 Me n-Bu 2 CF(CF₃)₂ 1-214 Me i-Bu 2 CF(CF₃)₂ 1-215 Me s-Bu 2 CF(CF₃)₂ 1-216 Me t-Bu 2 CF(CF₃)₂ 1-217 Et Me 0 CF(CF₃)₂ 1-218 Et Et 0 CF(CF₃)₂ 1-219 Et n-Pr 0 CF(CF₃)₂ 1-220 Et i-Pr 0 CF(CF₃)₂ 1-221 Et n-Bu 0 CF(CF₃)₂ 1-222 Et i-Bu 0 CF(CF₃)₂ 1-223 Et s-Bu 0 CF(CF₃)₂ 1-224 Et t-Bu 0 CF(CF₃)₂ 1-225 Et Me 1 CF(CF₃)₂ 1-226 Et Et 1 CF(CF₃)₂ 1-227 Et n-Pr 1 CF(CF₃)₂ 1-228 Et i-Pr 1 CF(CF₃)₂ 1-229 Et n-Bu 1 CF(CF₃)₂ 1-230 Et i-Bu 1 CF(CF₃)₂ 1-231 Et s-Bu 1 CF(CF₃)₂ 1-232 Et t-Bu 1 CF(CF₃)₂ 1-233 Et Me 2 CF(CF₃)₂ 1-234 Et Et 2 CF(CF₃)₂ 1-235 Et n-Pr 2 CF(CF₃)₂ 1-236 Et i-Pr 2 CF(CF₃)₂ 1-237 Et n-Bu 2 CF(CF₃)₂ 1-238 Et i-Bu 2 CF(CF₃)₂ 1-239 Et s-Bu 2 CF(CF₃)₂ 1-240 Et t-Bu 2 CF(CF₃)₂ 1-241 Me Me 0 CHF₂ 1-242 Me Et 0 CHF₂ 1-243 Me n-Pr 0 CHF₂ 1-244 Me i-Pr 0 CHF₂ 1-245 Me n-Bu 0 CHF₂ 1-246 Me i-Bu 0 CHF₂ 1-247 Me s-Bu 0 CHF₂ 1-248 Me t-Bu 0 CHF₂ 1-249 Me Me 1 CHF₂ 1-250 Me Et 1 CHF₂ 1-251 Me n-Pr 1 CHF₂ 1-252 Me i-Pr 1 CHF₂ 1-253 Me n-Bu 1 CHF₂ 1-254 Me i-Bu 1 CHF₂ 1-255 Me s-Bu 1 CHF₂ 1-256 Me t-Bu 1 CHF₂ 1-257 Me Me 2 CHF₂ 1-258 Me Et 2 CHF₂ 1-259 Me n-Pr 2 CHF₂ 1-260 Me i-Pr 2 CHF₂ 1-261 Me n-Bu 2 CHF₂ 1-262 Me i-Bu 2 CHF₂ 1-263 Me s-Bu 2 CHF₂ 1-264 Me t-Bu 0 CHF₂ 1-265 Et Me 0 CHF₂ 1-266 Et Et 0 CHF₂ 1-267 Et n-Pr 0 CHF₂ 1-268 Et i-Pr 0 CHF₂ 1-269 Et n-Bu 0 CHF₂ 1-270 Et i-Bu 0 CHF₂ 1-271 Et s-Bu 0 CHF₂ 1-272 Et t-Bu 0 CHF₂ 1-273 Et Me 1 CHF₂ 1-274 Et Et 1 CHF₂ 1-755 Et n-Pr 1 CHF₂ 1-276 Et i-Pr 1 CHF₂ 1-277 Et n-Bu 1 CHF₂ 1-278 Et i-Bu 1 CHF₂ 1-279 Et s-Bu 1 CHF₂ 1-280 Et t-Bu 1 CHF₂ 1-281 Et Me 2 CHF₂ 1-282 Et Et 2 CHF₂ 1-283 Et n-Pr 2 CHF₂ 1-284 Et i-Pr 2 CHF₂ 1-285 Et n-Bu 2 CHF₂ 1-286 Et i-Bu 2 CHF₂ 1-287 Et s-Bu 2 CHF₂ 1-288 Et t-Bu 2 CHF₂

TABLE 2 Inventive compounds of the formula (I) in which R² is ethyl, and R³ and R⁴ are each hydrogen

Physical data: No. X R¹ n Y ¹H-NMR: δ [CDCl₃] 2-1 Me Me 0 CF₂Cl 2-2 Me Et 0 CF₂Cl 2-3 Me n-Pr 0 CF₂Cl 2-4 Me i-Pr 0 CF₂Cl 2-5 Me n-Bu 0 CF₂Cl 2-6 Me i-Bu 0 CF₂Cl 2-7 Me s-Bu 0 CF₂Cl 2-8 Me t-Bu 0 CF₂Cl 2-9 Me Me 1 CF₂Cl 2-10 Me Et 1 CF₂Cl 2-11 Me n-Pr 1 CF₂Cl 2-12 Me i-Pr 1 CF₂Cl 2-13 Me n-Bu 1 CF₂Cl 2-14 Me i-Bu 1 CF₂Cl 2-15 Me s-Bu 1 CF₂Cl 2-16 Me t-Bu 1 CF₂Cl 2-17 Me Me 2 CF₂Cl 2-18 Me Et 2 CF₂Cl 2-19 Me n-Pr 2 CF₂Cl 2-20 Me i-Pr 2 CF₂Cl 2-21 Me n-Bu 2 CF₂Cl 2-22 Me i-Bu 2 CF₂Cl 2-23 Me s-Bu 2 CF₂Cl 2-24 Me t-Bu 2 CF₂Cl 2-25 Et Me 0 CF₂Cl 2-26 Et Et 0 CF₂Cl 2-27 Et n-Pr 0 CF₂Cl 2-28 Et i-Pr 0 CF₂Cl 2-29 Et n-Bu 0 CF₂Cl 2-30 Et i-Bu 0 CF₂Cl 2-31 Et s-Bu 0 CF₂Cl 2-32 Et t-Bu 0 CF₂Cl 2-33 Et Me 1 CF₂Cl 2-34 Et Et 1 CF₂Cl 2-35 Et n-Pr 1 CF₂Cl 2-36 Et i-Pr 1 CF₂Cl 2-37 Et n-Bu 1 CF₂Cl 2-38 Et i-Bu 1 CF₂Cl 2-39 Et s-Bu 1 CF₂Cl 2-40 Et t-Bu 1 CF₂Cl 2-41 Et Me 2 CF₂Cl 2-42 Et Et 2 CF₂Cl 2-43 Et n-Pr 2 CF₂Cl 2-44 Et i-Pr 2 CF₂Cl 2-45 Et n-Bu 2 CF₂Cl 2-46 Et i-Bu 2 CF₂Cl 2-47 Et s-Bu 2 CF₂Cl 2-48 Et t-Bu 2 CF₂Cl 2-49 Me Me 0 CFCl₂ 2-50 Me Et 0 CFCl₂ 2-51 Me n-Pr 0 CFCl₂ 2-52 Me i-Pr 0 CFCl₂ 2-53 Me n-Bu 0 CFCl₂ 2-54 Me i-Bu 0 CFCl₂ 2-55 Me s-Bu 0 CFCl₂ 2-56 Me t-Bu 0 CFCl₂ 2-57 Me Me 1 CFCl₂ 2-58 Me Et 1 CFCl₂ 2-59 Me n-Pr 1 CFCl₂ 2-60 Me i-Pr 1 CFCl₂ 2-61 Me n-Bu 1 CFCl₂ 2-62 Me i-Bu 1 CFCl₂ 2-63 Me s-Bu 1 CFCl₂ 2-64 Me t-Bu 1 CFCl₂ 2-65 Me Me 2 CFCl₂ 2-66 Me Et 2 CFCl₂ 2-67 Me n-Pr 2 CFCl₂ 2-68 Me i-Pr 2 CFCl₂ 2-69 Me n-Bu 2 CFCl₂ 2-70 Me i-Bu 2 CFCl₂ 2-71 Me s-Bu 2 CFCl₂ 2-72 Me t-Bu 2 CFCl₂ 2-73 Et Me 0 CFCl₂ 2-74 Et Et 0 CFCl₂ 2-75 Et n-Pr 0 CFCl₂ 2-76 Et i-Pr 0 CFCl₂ 2-77 Et n-Bu 0 CFCl₂ 2-78 Et i-Bu 0 CFCl₂ 2-79 Et s-Bu 0 CFCl₂ 2-80 Et t-Bu 0 CFCl₂ 2-81 Et Me 1 CFCl₂ 2-82 Et Et 1 CFCl₂ 2-83 Et n-Pr 1 CFCl₂ 2-84 Et i-Pr 1 CFCl₂ 2-85 Et n-Bu 1 CFCl₂ 2-86 Et i-Bu 1 CFCl₂ 2-87 Et s-Bu 1 CFCl₂ 2-88 Et t-Bu 1 CFCl₂ 2-89 Et Me 2 CFCl₂ 2-90 Et Et 2 CFCl₂ 2-91 Et n-Pr 2 CFCl₂ 2-92 Et i-Pr 2 CFCl₂ 2-93 Et n-Bu 2 CFCl₂ 2-94 Et i-Bu 2 CFCl₂ 2-95 Et s-Bu 2 CFCl₂ 2-96 Et t-Bu 2 CFCl₂ 2-97 Me Me 0 CCl₃ 2-98 Me Et 0 CCl₃ 2-99 Me n-Pr 0 CCl₃ 2-100 Me i-Pr 0 CCl₃ 2-101 Me n-Bu 0 CCl₃ 2-102 Me i-Bu 0 CCl₃ 2-103 Me s-Bu 0 CCl₃ 2-104 Me t-Bu 0 CCl₃ 2-105 Me Me 1 CCl₃ 2-106 Me Et 1 CCl₃ 2-107 Me n-Pr 1 CCl₃ 2-108 Me i-Pr 1 CCl₃ 2-109 Me n-Bu 1 CCl₃ 2-110 Me i-Bu 1 CCl₃ 2-111 Me s-Bu 1 CCl₃ 2-112 Me t-Bu 1 CCl₃ 2-113 Me Me 2 CCl₃ 2-114 Me Et 2 CCl₃ 2-115 Me n-Pr 2 CCl₃ 2-116 Me i-Pr 2 CCl₃ 2-117 Me n-Bu 2 CCl₃ 2-118 Me i-Bu 2 CCl₃ 2-119 Me s-Bu 2 CCl₃ 2-120 Me t-Bu 2 CCl₃ 2-121 Et Me 0 CCl₃ 2-122 Et Et 0 CCl₃ 2-123 Et n-Pr 0 CCl₃ 2-124 Et i-Pr 0 CCl₃ 2-125 Et n-Bu 0 CCl₃ 2-126 Et i-Bu 0 CCl₃ 2-127 Et s-Bu 0 CCl₃ 2-128 Et t-Bu 0 CCl₃ 2-129 Et Me 1 CCl₃ 2-130 Et Et 1 CCl₃ 2-131 Et n-Pr 1 CCl₃ 2-132 Et i-Pr 1 CCl₃ 2-133 Et n-Bu 1 CCl₃ 2-134 Et i-Bu 1 CCl₃ 2-135 Et s-Bu 1 CCl₃ 2-136 Et t-Bu 1 CCl₃ 2-137 Et Me 2 CCl₃ 2-138 Et Et 2 CCl₃ 2-139 Et n-Pr 2 CCl₃ 2-140 Et i-Pr 2 CCl₃ 2-141 Et n-Bu 2 CCl₃ 2-142 Et i-Bu 2 CCl₃ 2-143 Et s-Bu 2 CCl₃ 2-144 Et t-Bu 2 CCl₃ 2-145 Me Me 0 C₂F₅ 2-146 Me Et 0 C₂F₅ 2-147 Me n-Pr 0 C₂F₅ 2-148 Me i-Pr 0 C₂F₅ 2-149 Me n-Bu 0 C₂F₅ 2-150 Me i-Bu 0 C₂F₅ 2-151 Me s-Bu 0 C₂F₅ 2-152 Me t-Bu 0 C₂F₅ 2-153 Me Me 1 C₂F₅ 2-154 Me Et 1 C₂F₅ 2-155 Me n-Pr 1 C₂F₅ 2-156 Me i-Pr 1 C₂F₅ 2-157 Me n-Bu 1 C₂F₅ 2-158 Me i-Bu 1 C₂F₅ 2-159 Me s-Bu 1 C₂F₅ 2-160 Me t-Bu 1 C₂F₅ 2-161 Me Me 2 C₂F₅ 2-162 Me Et 2 C₂F₅ 2-163 Me n-Pr 2 C₂F₅ 2-164 Me i-Pr 2 C₂F₅ 2-165 Me n-Bu 2 C₂F₅ 2-166 Me i-Bu 2 C₂F₅ 2-167 Me s-Bu 2 C₂F₅ 2-168 Me t-Bu 2 C₂F₅ 2-169 Et Me 0 C₂F₅ 2-170 Et Et 0 C₂F₅ 2-171 Et n-Pr 0 C₂F₅ 2-172 Et i-Pr 0 C₂F₅ 2-173 Et n-Bu 0 C₂F₅ 2-174 Et i-Bu 0 C₂F₅ 2-175 Et s-Bu 0 C₂F₅ 2-176 Et t-Bu 0 C₂F₅ 2-177 Et Me 1 C₂F₅ 2-178 Et Et 1 C₂F₅ 2-179 Et n-Pr 1 C₂F₅ 2-180 Et i-Pr 1 C₂F₅ 2-181 Et n-Bu 1 C₂F₅ 2-182 Et i-Bu 1 C₂F₅ 2-183 Et s-Bu 1 C₂F₅ 2-184 Et t-Bu 1 C₂F₅ 2-185 Et Me 2 C₂F₅ 2-186 Et Et 2 C₂F₅ 2-187 Et n-Pr 2 C₂F₅ 2-188 Et i-Pr 2 C₂F₅ 2-189 Et n-Bu 2 C₂F₅ 2-190 Et i-Bu 2 C₂F₅ 2-191 Et s-Bu 2 C₂F₅ 2-192 Et t-Bu 2 C₂F₅ 2-193 Me Me 0 CF(CF₃)₂ 2-194 Me Et 0 CF(CF₃)₂ 2-195 Me n-Pr 0 CF(CF₃)₂ 2-196 Me i-Pr 0 CF(CF₃)₂ 2-197 Me n-Bu 0 CF(CF₃)₂ 2-198 Me i-Bu 0 CF(CF₃)₂ 2-199 Me s-Bu 0 CF(CF₃)₂ 2-200 Me t-Bu 0 CF(CF₃)₂ 2-201 Me Me 1 CF(CF₃)₂ 2-202 Me Et 1 CF(CF₃)₂ 2-203 Me n-Pr 1 CF(CF₃)₂ 2-204 Me i-Pr 1 CF(CF₃)₂ 2-205 Me n-Bu 1 CF(CF₃)₂ 2-206 Me i-Bu 1 CF(CF₃)₂ 2-207 Me s-Bu 1 CF(CF₃)₂ 2-208 Me t-Bu 1 CF(CF₃)₂ 2-209 Me Me 2 CF(CF₃)₂ 2-210 Me Et 2 CF(CF₃)₂ 2-211 Me n-Pr 2 CF(CF₃)₂ 2-212 Me i-Pr 2 CF(CF₃)₂ 2-213 Me n-Bu 2 CF(CF₃)₂ 2-214 Me i-Bu 2 CF(CF₃)₂ 2-215 Me s-Bu 2 CF(CF₃)₂ 2-216 Me t-Bu 2 CF(CF₃)₂ 2-217 Et Me 0 CF(CF₃)₂ 2-218 Et Et 0 CF(CF₃)₂ 2-219 Et n-Pr 0 CF(CF₃)₂ 2-220 Et i-Pr 0 CF(CF₃)₂ 2-221 Et n-Bu 0 CF(CF₃)₂ 2-222 Et i-Bu 0 CF(CF₃)₂ 2-223 Et s-Bu 0 CF(CF₃)₂ 2-224 Et t-Bu 0 CF(CF₃)₂ 2-225 Et Me 1 CF(CF₃)₂ 2-226 Et Et 1 CF(CF₃)₂ 2-227 Et n-Pr 1 CF(CF₃)₂ 2-228 Et i-Pr 1 CF(CF₃)₂ 2-229 Et n-Bu 1 CF(CF₃)₂ 2-230 Et i-Bu 1 CF(CF₃)₂ 2-231 Et s-Bu 1 CF(CF₃)₂ 2-232 Et t-Bu 1 CF(CF₃)₂ 2-233 Et Me 2 CF(CF₃)₂ 2-234 Et Et 2 CF(CF₃)₂ 2-235 Et n-Pr 2 CF(CF₃)₂ 2-236 Et i-Pr 2 CF(CF₃)₂ 2-237 Et n-Bu 2 CF(CF₃)₂ 2-238 Et i-Bu 2 CF(CF₃)₂ 2-239 Et s-Bu 2 CF(CF₃)₂ 2-240 Et t-Bu 2 CF(CF₃)₂ 2-241 Me Me 0 CHF₂ 2-242 Me Et 0 CHF₂ 2-243 Me n-Pr 0 CHF₂ 2-244 Me i-Pr 0 CHF₂ 2-245 Me n-Bu 0 CHF₂ 2-246 Me i-Bu 0 CHF₂ 2-247 Me s-Bu 0 CHF₂ 2-248 Me t-Bu 0 CHF₂ 2-249 Me Me 1 CHF₂ 2-250 Me Et 1 CHF₂ 2-251 Me n-Pr 1 CHF₂ 2-252 Me i-Pr 1 CHF₂ 2-253 Me n-Bu 1 CHF₂ 2-254 Me i-Bu 1 CHF₂ 2-255 Me s-Bu 1 CHF₂ 2-256 Me t-Bu 1 CHF₂ 2-257 Me Me 2 CHF₂ 2-258 Me Et 2 CHF₂ 2-259 Me n-Pr 2 CHF₂ 2-260 Me i-Pr 2 CHF₂ 2-261 Me n-Bu 2 CHF₂ 2-262 Me i-Bu 2 CHF₂ 2-263 Me s-Bu 2 CHF₂ 2-264 Me t-Bu 2 CHF₂ 2-265 Et Me 0 CHF₂ 2-266 Et Et 0 CHF₂ 2-267 Et n-Pr 0 CHF₂ 2-268 Et i-Pr 0 CHF₂ 2-269 Et n-Bu 0 CHF₂ 2-270 Et i-Bu 0 CHF₂ 2-271 Et s-Bu 0 CHF₂ 2-272 Et t-Bu 0 CHF₂ 2-273 Et Me 1 CHF₂ 2-274 Et Et 1 CHF₂ 2-275 Et n-Pr 1 CHF₂ 2-276 Et i-Pr 1 CHF₂ 2-277 Et n-Bu 1 CHF₂ 2-278 Et i-Bu 1 CHF₂ 2-279 Et s-Bu 1 CHF₂ 2-280 Et t-Bu 1 CHF₂ 2-281 Et Me 2 CHF₂ 2-282 Et Et 2 CHF₂ 2-283 Et n-Pr 2 CHF₂ 2-284 Et i-Pr 2 CHF₂ 2-285 Et n-Bu 2 CHF₂ 2-286 Et i-Bu 2 CHF₂ 2-287 Et s-Bu 2 CHF₂ 2-288 Et t-Bu 2 CHF₂

TABLE 3 Inventive compounds of the formula (I) in which R² and R³ are methyl, and R⁴ is hydrogen

Physical data: No. X R¹ n Y ¹H-NMR: δ [CDCl₃] 3-1 Me Me 0 CF₂Cl 3-2 Me Et 0 CF₂Cl 3-3 Me n-Pr 0 CF₂Cl 3-4 Me i-Pr 0 CF₂Cl 3-5 Me n-Bu 0 CF₂Cl 3-6 Me i-Bu 0 CF₂Cl 3-7 Me s-Bu 0 CF₂Cl 3-8 Me t-Bu 0 CF₂Cl 3-9 Me Me 1 CF₂Cl 3-10 Me Et 1 CF₂Cl 3-11 Me n-Pr 1 CF₂Cl 3-12 Me i-Pr 1 CF₂Cl 3-13 Me n-Bu 1 CF₂Cl 3-14 Me i-Bu 1 CF₂Cl 3-15 Me s-Bu 1 CF₂Cl 3-16 Me t-Bu 1 CF₂Cl 3-17 Me Me 2 CF₂Cl 3-18 Me Et 2 CF₂Cl 3-19 Me n-Pr 2 CF₂Cl 3-20 Me i-Pr 2 CF₂Cl 3-21 Me n-Bu 2 CF₂Cl 3-22 Me i-Bu 2 CF₂Cl 3-23 Me s-Bu 2 CF₂Cl 3-24 Me t-Bu 2 CF₂Cl 3-25 Et Me 0 CF₂Cl 3-26 Et Et 0 CF₂Cl 3-27 Et n-Pr 0 CF₂Cl 3-28 Et i-Pr 0 CF₂Cl 3-29 Et n-Bu 0 CF₂Cl 3-30 Et i-Bu 0 CF₂Cl 3-31 Et s-Bu 0 CF₂Cl 3-32 Et t-Bu 0 CF₂Cl 3-33 Et Me 1 CF₂Cl 3-34 Et Et 1 CF₂Cl 3-35 Et n-Pr 1 CF₂Cl 3-36 Et i-Pr 1 CF₂Cl 3-37 Et n-Bu 1 CF₂Cl 3-38 Et i-Bu 1 CF₂Cl 3-39 Et s-Bu 1 CF₂Cl 3-40 Et t-Bu 1 CF₂Cl 3-41 Et Me 2 CF₂Cl 3-42 Et Et 2 CF₂Cl 3-43 Et n-Pr 2 CF₂Cl 3-44 Et i-Pr 2 CF₂Cl 3-45 Et n-Bu 2 CF₂Cl 3-46 Et i-Bu 2 CF₂Cl 3-47 Et s-Bu 2 CF₂Cl 3-48 Et t-Bu 2 CF₂Cl 3-49 Me Me 0 CFCl₂ 3-50 Me Et 0 CFCl₂ 3-51 Me n-Pr 0 CFCl₂ 3-52 Me i-Pr 0 CFCl₂ 3-53 Me n-Bu 0 CFCl₂ 3-54 Me i-Bu 0 CFCl₂ 3-55 Me s-Bu 0 CFCl₂ 3-56 Me t-Bu 0 CFCl₂ 3-57 Me Me 1 CFCl₂ 3-58 Me Et 1 CFCl₂ 3-59 Me n-Pr 1 CFCl₂ 3-60 Me i-Pr 1 CFCl₂ 3-61 Me n-Bu 1 CFCl₂ 3-62 Me i-Bu 1 CFCl₂ 3-63 Me s-Bu 1 CFCl₂ 3-64 Me t-Bu 1 CFCl₂ 3-65 Me Me 2 CFCl₂ 3-66 Me Et 2 CFCl₂ 3-67 Me n-Pr 2 CFCl₂ 3-68 Me i-Pr 2 CFCl₂ 3-69 Me n-Bu 2 CFCl₂ 3-70 Me i-Bu 2 CFCl₂ 3-71 Me s-Bu 2 CFCl₂ 3-72 Me t-Bu 2 CFCl₂ 3-73 Et Me 0 CFCl₂ 3-74 Et Et 0 CFCl₂ 3-75 Et n-Pr 0 CFCl₂ 3-76 Et i-Pr 0 CFCl₂ 3-77 Et n-Bu 0 CFCl₂ 3-78 Et i-Bu 0 CFCl₂ 3-79 Et s-Bu 0 CFCl₂ 3-80 Et t-Bu 0 CFCl₂ 3-81 Et Me 1 CFCl₂ 3-82 Et Et 1 CFCl₂ 3-83 Et n-Pr 1 CFCl₂ 3-84 Et i-Pr 1 CFCl₂ 3-85 Et n-Bu 1 CFCl₂ 3-86 Et i-Bu 1 CFCl₂ 3-87 Et s-Bu 1 CFCl₂ 3-88 Et t-Bu 1 CFCl₂ 3-89 Et Me 2 CFCl₂ 3-90 Et Et 2 CFCl₂ 3-91 Et n-Pr 2 CFCl₂ 3-92 Et i-Pr 2 CFCl₂ 3-93 Et n-Bu 2 CFCl₂ 3-94 Et i-Bu 2 CFCl₂ 3-95 Et s-Bu 2 CFCl₂ 3-96 Et t-Bu 2 CFCl₂ 3-97 Me Me 0 CCl₃ 3-98 Me Et 0 CCl₃ 3-99 Me n-Pr 0 CCl₃ 3-100 Me i-Pr 0 CCl₃ 3-101 Me n-Bu 0 CCl₃ 3-102 Me i-Bu 0 CCl₃ 3-103 Me s-Bu 0 CCl₃ 3-104 Me t-Bu 0 CCl₃ 3-105 Me Me 1 CCl₃ 3-106 Me Et 1 CCl₃ 3-107 Me n-Pr 1 CCl₃ 3-108 Me i-Pr 1 CCl₃ 3-109 Me n-Bu 1 CCl₃ 3-110 Me i-Bu 1 CCl₃ 3-111 Me s-Bu 1 CCl₃ 3-112 Me t-Bu 1 CCl₃ 3-113 Me Me 2 CCl₃ 3-114 Me Et 2 CCl₃ 3-115 Me n-Pr 2 CCl₃ 3-116 Me i-Pr 2 CCl₃ 3-117 Me n-Bu 2 CCl₃ 3-118 Me i-Bu 2 CCl₃ 3-119 Me s-Bu 2 CCl₃ 3-120 Me t-Bu 2 CCl₃ 3-121 Et Me 0 CCl₃ 3-122 Et Et 0 CCl₃ 3-123 Et n-Pr 0 CCl₃ 3-124 Et i-Pr 0 CCl₃ 3-125 Et n-Bu 0 CCl₃ 3-126 Et i-Bu 0 CCl₃ 3-127 Et s-Bu 0 CCl₃ 3-128 Et t-Bu 0 CCl₃ 3-129 Et Me 1 CCl₃ 3-130 Et Et 1 CCl₃ 3-131 Et n-Pr 1 CCl₃ 3-132 Et i-Pr 1 CCl₃ 3-133 Et n-Bu 1 CCl₃ 3-134 Et i-Bu 1 CCl₃ 3-135 Et s-Bu 1 CCl₃ 3-136 Et t-Bu 1 CCl₃ 3-137 Et Me 2 CCl₃ 3-138 Et Et 2 CCl₃ 3-139 Et n-Pr 2 CCl₃ 3-140 Et i-Pr 2 CCl₃ 3-141 Et n-Bu 2 CCl₃ 3-142 Et i-Bu 2 CCl₃ 3-143 Et s-Bu 2 CCl₃ 3-144 Et t-Bu 2 CCl₃ 3-145 Me Me 0 C₂F₅ 7.62 (d, 1H), 7.31 (d, 1H), 3.64 (s, 3H), 2.61 (s, 3H), 2.28 (s, 3H), 1.63 (s, 3H) 3-146 Me Et 0 C₂F₅ 3-147 Me n-Pr 0 C₂F₅ 3-148 Me i-Pr 0 C₂F₅ 3-149 Me n-Bu 0 C₂F₅ 3-150 Me i-Bu 0 C₂F₅ 3-151 Me s-Bu 0 C₂F₅ 3-151 Me t-Bu 0 C₂F₅ 3-153 Me Me 1 C₂F₅ 7.63 (d, 1H), 7.43 (d, 1H), 3.66 (s, 3H), 3.03 (s, 3H), 2.86 (s, 3H), 1.67 (s, 3H) 3-154 Me Et 1 C₂F₅ 3-155 Me n-Pr 1 C₂F₅ 3-156 Me i-Pr 1 C₂F₅ 3-157 Me n-Bu 1 C₂F₅ 3-158 Me i-Bu 1 C₂F₅ 3-159 Me s-Bu 1 C₂F₅ 3-160 Me t-Bu 1 C₂F₅ 3-161 Me Me 2 C₂F₅ 7.77 (d, 1H), 7.53 (d, 1H), 3.66 (s, 3H), 3.28 (s, 3H), 2.72 (s, 3H), 1.68 (s, 3H) 3-162 Me Et 2 C₂F₅ 3-163 Me n-Pr 2 C₂F₅ 3-164 Me i-Pr 2 C₂F₅ 3-165 Me n-Bu 2 C₂F₅ 3-166 Me i-Bu 2 C₂F₅ 3-167 Me s-Bu 2 C₂F₅ 3-168 Me t-Bu 2 C₂F₅ 3-169 Et Me 0 C₂F₅ 3-170 Et Et 0 C₂F₅ 3-171 Et n-Pr 0 C₂F₅ 3-172 Et i-Pr 0 C₂F₅ 3-173 Et n-Bu 0 C₂F₅ 3-174 Et i-Bu 0 C₂F₅ 3-175 Et s-Bu 0 C₂F₅ 3-176 Et t-Bu 0 C₂F₅ 3-177 Et Me 1 C₂F₅ 3-178 Et Et 1 C₂F₅ 3-179 Et n-Pr 1 C₂F₅ 3-180 Et i-Pr 1 C₂F₅ 3-181 Et n-Bu 1 C₂F₅ 3-182 Et i-Bu 1 C₂F₅ 3-183 Et s-Bu 1 C₂F₅ 3-184 Et t-Bu 1 C₂F₅ 3-185 Et Me 2 C₂F₅ 3-186 Et Et 2 C₂F₅ 3-187 Et n-Pr 2 C₂F₅ 3-188 Et i-Pr 2 C₂F₅ 3-189 Et n-Bu 2 C₂F₅ 3-190 Et i-Bu 2 C₂F₅ 3-191 Et s-Bu 2 C₂F₅ 3-192 Et t-Bu 2 C₂F₅ 3-193 Me Me 0 CF(CF₃)₂ 3-194 Me Et 0 CF(CF₃)₂ 3-195 Me n-Pr 0 CF(CF₃)₂ 3-196 Me i-Pr 0 CF(CF₃)₂ 3-197 Me n-Bu 0 CF(CF₃)₂ 3-198 Me i-Bu 0 CF(CF₃)₂ 3-199 Me s-Bu 0 CF(CF₃)₂ 3-200 Me t-Bu 0 CF(CF₃)₂ 3-201 Me Me 1 CF(CF₃)₂ 3-202 Me Et 1 CF(CF₃)₂ 3-203 Me n-Pr 1 CF(CF₃)₂ 3-204 Me i-Pr 1 CF(CF₃)₂ 3-205 Me n-Bu 1 CF(CF₃)₂ 3-206 Me i-Bu 1 CF(CF₃)₂ 3-207 Me s-Bu 1 CF(CF₃)₂ 3-208 Me t-Bu 1 CF(CF₃)₂ 3-209 Me Me 2 CF(CF₃)₂ 3-210 Me Et 2 CF(CF₃)₂ 3-211 Me n-Pr 2 CF(CF₃)₂ 3-212 Me i-Pr 2 CF(CF₃)₂ 3-213 Me n-Bu 2 CF(CF₃)₂ 3-214 Me i-Bu 2 CF(CF₃)₂ 3-215 Me s-Bu 2 CF(CF₃)₂ 3-216 Me t-Bu 2 CF(CF₃)₂ 3-217 Et Me 0 CF(CF₃)₂ 3-218 Et Et 0 CF(CF₃)₂ 3-219 Et n-Pr 0 CF(CF₃)₂ 3-220 Et i-Pr 0 CF(CF₃)₂ 3-221 Et n-Bu 0 CF(CF₃)₂ 3-222 Et i-Bu 0 CF(CF₃)₂ 3-223 Et s-Bu 0 CF(CF₃)₂ 3-224 Et t-Bu 0 CF(CF₃)₂ 3-225 Et Me 1 CF(CF₃)₂ 3-226 Et Et 1 CF(CF₃)₂ 3-227 Et n-Pr 1 CF(CF₃)₂ 3-228 Et i-Pr 1 CF(CF₃)₂ 3-229 Et n-Bu 1 CF(CF₃)₂ 3-230 Et i-Bu 1 CF(CF₃)₂ 3-231 Et s-Bu 1 CF(CF₃)₂ 3-232 Et t-Bu 1 CF(CF₃)₂ 3-233 Et Me 2 CF(CF₃)₂ 3-234 Et Et 2 CF(CF₃)₂ 3-235 Et n-Pr 2 CF(CF₃)₂ 3-236 Et i-Pr 2 CF(CF₃)₂ 3-237 Et n-Bu 2 CF(CF₃)₂ 3-238 Et i-Bu 2 CF(CF₃)₂ 3-239 Et s-Bu 2 CF(CF₃)₂ 3-240 Et t-Bu 2 CF(CF₃)₂ 3-241 Me Me 0 CHF₂ 3-242 Me Et 0 CHF₂ 3-243 Me n-Pr 0 CHF₂ 3-244 Me i-Pr 0 CHF₂ 3-245 Me n-Bu 0 CHF₂ 3-246 Me i-Bu 0 CHF₂ 3-247 Me s-Bu 0 CHF₂ 3-248 Me t-Bu 0 CHF₂ 3-249 Me Me 1 CHF₂ 3-250 Me Et 1 CHF₂ 3-251 Me n-Pr 1 CHF₂ 3-252 Me i-Pr 1 CHF₂ 3-253 Me n-Bu 1 CHF₂ 3-254 Me i-Bu 1 CHF₂ 3-255 Me s-Bu 1 CHF₂ 3-256 Me t-Bu 1 CHF₂ 3-257 Me Me 2 CHF₂ 3-258 Me Et 2 CHF₂ 3-259 Me n-Pr 2 CHF₂ 3-260 Me i-Pr 2 CHF₂ 3-261 Me n-Bu 2 CHF₂ 3-262 Me i-Bu 2 CHF₂ 3-263 Me s-Bu 2 CHF₂ 3-264 Me t-Bu 2 CHF₂ 3-265 Et Me 0 CHF₂ 3-266 Et Et 0 CHF₂ 3-267 Et n-Pr 0 CHF₂ 3-268 Et i-Pr 0 CHF₂ 3-269 Et n-Bu 0 CHF₂ 3-270 Et i-Bu 0 CHF₂ 3-271 Et s-Bu 0 CHF₂ 3-272 Et t-Bu 0 CHF₂ 3-273 Et Me 1 CHF₂ 3-274 Et Et 1 CHF₂ 3-275 Et n-Pr 1 CHF₂ 3-276 Et i-Pr 1 CHF₂ 3-277 Et n-Bu 1 CHF₂ 3-278 Et i-Bu 1 CHF₂ 3-279 Et s-Bu 1 CHF₂ 3-280 Et t-Bu 1 CHF₂ 3-281 Et Me 2 CHF₂ 3-282 Et Et 2 CHF₂ 3-283 Et n-Pr 2 CHF₂ 3-284 Et i-Pr 2 CHF₂ 3-285 Et n-Bu 2 CHF₂ 3-286 Et i-Bu 2 CHF₂ 3-287 Et s-Bu 2 CHF₂ 3-288 Et t-Bu 2 CHF₂

TABLE 4 Inventive compounds of the formula (I)

Physical data: No. R² R³ X R¹ n Y R⁴ ¹H-NMR: δ [CDCl₃] 4-1 Me H Me Me 0 CF₂Cl —SO₂-n-Pr 4-2 Me H Me Et 0 CF₂Cl —SO₂-n-Pr 4-3 Me H Me n-Pr 0 CF₂Cl —SO₂-n-Pr 4-4 Me H Me Me 1 CF₂Cl —SO₂-n-Pr 4-5 Me H Me Et 1 CF₂Cl —SO₂-n-Pr 4-6 Me H Me n-Pr 1 CF₂Cl —SO₂-n-Pr 4-7 Me H Me Me 2 CF₂Cl —SO₂-n-Pr 4-8 Me H Me Et 2 CF₂Cl —SO₂-n-Pr 4-9 Me H Me n-Pr 2 CF₂Cl —SO₂-n-Pr 4-10 Me H Me Me 0 CF₂Cl —SO₂—(CH₂)₂OMe 4-11 Me H Me Et 0 CF₂Cl —SO₂—(CH₂)₂OMe 4-12 Me H Me n-Pr 0 CF₂Cl —SO₂—(CH₂)₂OMe 4-13 Me H Me Me 1 CF₂Cl —SO₂—(CH₂)₂OMe 4-14 Me H Me Et 1 CF₂Cl —SO₂—(CH₂)₂OMe 4-15 Me H Me n-Pr 1 CF₂Cl —SO₂—(CH₂)₂OMe 4-16 Me H Me Me 2 CF₂Cl —SO₂—(CH₂)₂OMe 4-17 Me H Me Et 2 CF₂Cl —SO₂—(CH₂)₂OMe 4-18 Me H Me n-Pr 2 CF₂Cl —SO₂—(CH₂)₂OMe 4-19 Me H Me Me 0 CF₂Cl —SO₂—Ph 4-20 Me H Me Et 0 CF₂Cl —SO₂—Ph 4-21 Me H Me n-Pr 0 CF₂Cl —SO₂—Ph 4-22 Me H Me Me 1 CF₂Cl —SO₂—Ph 4-23 Me H Me Et 1 CF₂Cl —SO₂—Ph 4-24 Me H Me n-Pr 1 CF₂Cl —SO₂—Ph 4-25 Me H Me Me 2 CF₂Cl —SO₂—Ph 4-26 Me H Me Et 2 CF₂Cl —SO₂—Ph 4-27 Me H Me n-Pr 2 CF₂Cl —SO₂—Ph 4-28 Me H Me Me 0 CF₂Cl —SO₂-(4-Me—Ph) 4-29 Me H Me Et 0 CF₂Cl —SO₂-(4-Me—Ph) 4-30 Me H Me n-Pr 0 CF₂Cl —SO₂-(4-Me—Ph) 4-31 Me H Me Me 1 CF₂Cl —SO₂-(4-Me—Ph) 4-32 Me H Me Et 1 CF₂Cl —SO₂-—(4-Me—Ph) 4-33 Me H Me n-Pr 1 CF₂Cl —SO₂-(4-Me—Ph) 4-34 Me H Me Me 2 CF₂Cl —SO₂-(4-Me—Ph) 4-35 Me H Me Et 2 CF₂Cl —SO₂-—(4-Me—Ph) 4-36 Me H Me n-Pr 2 CF₂Cl —SO₂-—(4-Me—Ph) 4-37 Me H Me Me 0 CF₂Cl —SO₂-(Thien-2-yl) 4-38 Me H Me Et 0 CF₂Cl —SO₂-(Thien-2-yl) 4-39 Me H Me n-Pr 0 CF₂Cl —SO₂-(Thien-2-yl) 4-40 Me H Me Me 1 CF₂Cl —SO₂-(Thien-2-yl) 4-41 Me H Me Et 1 CF₂Cl —SO₂-(Thien-2-yl) 4-42 Me H Me n-Pr 1 CF₂Cl —SO₂-(Thien-2-yl) 4-43 Me H Me Me 2 CF₂Cl —SO₂-(Thien-2-yl) 4-44 Me H Me Et 2 CF₂Cl —SO₂-(Thien-2-yl) 4-45 Me H Me n-Pr 2 CF₂Cl —SO₂-(Thien-2-yl) 4-46 Me H Me Me 0 CF₂Cl —CO—Ph 4-47 Me H Me Et 0 CF₂Cl —CO—Ph 4-48 Me H Me n-Pr 0 CF₂Cl —CO—Ph 4-49 Me H Me Me 1 CF₂Cl —CO—Ph 4-50 Me H Me Et 1 CF₂Cl —CO—Ph 4-51 Me H Me n-Pr 1 CF₂Cl —CO—Ph 4-52 Me H Me Me 2 CF₂Cl —CO—Ph 4-53 Me H Me Et 2 CF₂Cl —CO—Ph 4-54 Me H Me n-Pr 2 CF₂Cl —CO—Ph 4-55 Me H Me Me 0 CF₂Cl —CH₂—CO—Ph 4-56 Me H Me Et 0 CF₂Cl —CH₂—CO—Ph 4-57 Me H Me n-Pr 0 CF₂Cl —CH₂—CO—Ph 4-58 Me H Me Me 1 CF₂Cl —CH₂—CO—Ph 4-59 Me H Me Et 1 CF₂Cl —CH₂—CO—Ph 4-60 Me H Me n-Pr 1 CF₂Cl —CH₂—CO—Ph 4-61 Me H Me Me 2 CF₂Cl —CH₂—CO—Ph 4-62 Me H Me Et 2 CF₂Cl —CH₂—CO—Ph 4-63 Me H Me n-Pr 2 CF₂Cl —CH₂—CO—Ph 4-64 Et H Me Me 0 CF₂Cl —SO₂—n-Pr 4-65 Et H Me Et 0 CF₂Cl —SO₂—n-Pr 4-66 Et H Me n-Pr 0 CF₂Cl —SO₂—n-Pr 4-67 Et H Me Me 1 CF₂Cl —SO₂—n-Pr 4-68 Et H Me Et 1 CF₂Cl —SO₂—n-Pr 4-69 Et H Me n-Pr 1 CF₂Cl —SO₂—n-Pr 4-70 Et H Me Me 2 CF₂Cl —SO₂—n-Pr 4-71 Et H Me Et 2 CF₂Cl —SO₂—n-Pr 4-72 Et H Me n-Pr 2 CF₂Cl —SO₂—n-Pr 4-73 Et H Me Me 0 CF₂Cl —SO₂—(CH₂)₂OMe 4-74 Et H Me Et 0 CF₂Cl —SO₂—(CH₂)₂OMe 4-75 Et H Me n-Pr 0 CF₂Cl —SO₂—(CH₂)₂OMe 4-76 Et H Me Me 1 CF₂Cl —SO₂—(CH₂)₂OMe 4-77 Et H Me Et 1 CF₂Cl —SO₂—(CH₂)₂OMe 4-78 Et H Me n-Pr 1 CF₂Cl —SO₂—(CH₂)₂OMe 4-79 Et H Me Me 2 CF₂Cl —SO₂—(CH₂)₂OMe 4-80 Et H Me Et 2 CF₂Cl —SO₂—(CH₂)₂OMe 4-81 Et H Me n-Pr 2 CF₂Cl —SO₂—(CH₂)₂OMe 4-82 Et H Me Me 0 CF₂Cl —SO₂—Ph 4-83 Et H Me Et 0 CF₂Cl —SO₂—Ph 4-84 Et H Me n-Pr 0 CF₂Cl —SO₂—Ph 4-85 Et H Me Me 1 CF₂Cl —SO₂—Ph 4-86 Et H Me Et 1 CF₂Cl —SO₂—Ph 4-87 Et H Me n-Pr 1 CF₂Cl —SO₂—Ph 4-88 Et H Me Me 2 CF₂Cl —SO₂—Ph 4-89 Et H Me Et 2 CF₂Cl —SO₂—Ph 4-90 Et H Me n-Pr 2 CF₂Cl —SO₂—Ph 4-91 Et H Me Me 0 CF₂Cl —SO₂—(4-Me—Ph) 4-92 Et H Me Et 0 CF₂Cl —SO₂—(4-Me—Ph) 4-93 Et H Me n-Pr 0 CF₂Cl —SO₂—(4-Me—Ph) 4-94 Et H Me Me 1 CF₂Cl —SO₂—(4-Me—Ph) 4-95 Et H Me Et 1 CF₂Cl —SO₂—(4-Me—Ph) 4-96 Et H Me n-Pr 1 CF₂Cl —SO₂—(4-Me—Ph) 4-97 Et H Me Me 2 CF₂Cl —SO₂—(4-Me—Ph) 4-98 Et H Me Et 2 CF₂Cl —SO₂—(4-Me—Ph) 4-99 Et H Me n-Pr 2 CF₂Cl —SO₂—(4-Me—Ph) 4-100 Et H Me Me 0 CF₂Cl —SO₂-(Thien-2-yl) 4-101 Et H Me Et 0 CF₂Cl —SO₂-(Thien-2-yl) 4-102 Et H Me n-Pr 0 CF₂Cl —SO₂-(Thien-2-yl) 4-103 Et H Me Me 1 CF₂Cl —SO₂-(Thien-2-yl) 4-104 Et H Me Et 1 CF₂Cl —SO₂-(Thien-2-yl) 4-105 Et H Me n-Pr 1 CF₂Cl —SO₂-(Thien-2-yl) 4-106 Et H Me Me 2 CF₂Cl —SO₂-(Thien-2-yl) 4-107 Et H Me Et 2 CF₂Cl —SO₂-(Thien-2-yl) 4-108 Et H Me n-Pr 2 CF₂Cl —SO₂-(Thien-2-yl) 4-109 Et H Me Me 0 CF₂Cl —CO—Ph 4-110 Et H Me Et 0 CF₂Cl —CO—Ph 4-111 Et H Me n-Pr 0 CF₂Cl —CO—Ph 4-112 Et H Me Me 1 CF₂Cl —CO—Ph 4-113 Et H Me Et 1 CF₂Cl —CO—Ph 4-114 Et H Me n-Pr 1 CF₂Cl —CO—Ph 4-115 Et H Me Me 2 CF₂Cl —CO—Ph 4-116 Et H Me Et 2 CF₂Cl —CO—Ph 4-117 Et H Me n-Pr 2 CF₂Cl —CO—Ph 4-118 Et H Me Me 0 CF₂Cl —CH₂—CO—Ph 4-119 Et H Me Et 0 CF₂Cl —CH₂—CO—Ph 4-120 Et H Me n-Pr 0 CF₂Cl —CH₂—CO—Ph 4-121 Et H Me Me 1 CF₂Cl —CH₂—CO—Ph 4-122 Et H Me Et 1 CF₂Cl —CH₂—CO—Ph 4-123 Et H Me n-Pr 1 CF₂Cl —CH₂—CO—Ph 4-124 Et H Me Me 2 CF₂Cl —CH₂—CO—Ph 4-125 Et H Me Et 2 CF₂Cl —CH₂—CO—Ph 4-126 Et H Me n-Pr 2 CF₂Cl —CH₂—CO—Ph 4-127 Me Me Me Me 0 CF₂Cl —SO₂—n-Pr 4-128 Me Me Me Et 0 CF₂Cl —SO₂—n-Pr 4-129 Me Me Me n-Pr 0 CF₂Cl —SO₂—n-Pr 4-130 Me Me Me Me 1 CF₂Cl —SO₂—n-Pr 4-131 Me Me Me Et 1 CF₂Cl —SO₂—n-Pr 4-132 Me Me Me n-Pr 1 CF₂Cl —SO₂—n-Pr 4-133 Me Me Me Me 2 CF₂Cl —SO₂—n-Pr 4-134 Me Me Me Et 2 CF₂Cl —SO₂—n-Pr 4-135 Me Me Me n-Pr 2 CF₂Cl —SO₂—n-Pr 4-136 Me Me Me Me 0 CF₂Cl —SO₂—(CH₂)₂OMe 4-137 Me Me Me Et 0 CF₂Cl —SO₂—(CH₂)₂OMe 4-138 Me Me Me n-Pr 0 CF₂Cl —SO₂—(CH₂)₂OMe 4-139 Me Me Me Me 1 CF₂Cl —SO₂—(CH₂)₂OMe 4-140 Me Me Me Et 1 CF₂Cl —SO₂—(CH₂)₂OMe 4-141 Me Me Me n-Pr 1 CF₂Cl —SO₂—(CH₂)₂OMe 4-142 Me Me Me Me 2 CF₂Cl —SO₂—(CH₂)₂OMe 4-143 Me Me Me Et 2 CF₂Cl —SO₂—(CH₂)₂OMe 4-144 Me Me Me n-Pr 2 CF₂Cl —SO₂—(CH₂)₂OMe 4-145 Me Me Me Me 0 CF₂Cl —SO₂—Ph 4-146 Me Me Me Et 0 CF₂Cl —SO₂—Ph 4-147 Me Me Me n-Pr 0 CF₂Cl —SO₂—Ph 4-148 Me Me Me Me 1 CF₂Cl —SO₂—Ph 4-149 Me Me Me Et 1 CF₂Cl —SO₂—Ph 4-150 Me Me Me n-Pr 1 CF₂Cl —SO₂—Ph 4-151 Me Me Me Me 2 CF₂Cl —SO₂—Ph 4-152 Me Me Me Et 2 CF₂Cl —SO₂—Ph 4-153 Me Me Me n-Pr 2 CF₂Cl —SO₂—Ph 4-154 Me Me Me Me 0 CF₂Cl —SO₂—(4-Me—Ph) 4-155 Me Me Me Et 0 CF₂Cl —SO₂—(4-Me—Ph) 4-156 Me Me Me n-Pr 0 CF₂Cl —SO₂—(4-Me—Ph) 4-157 Me Me Me Me 1 CF₂Cl —SO₂—(4-Me—Ph) 4-158 Me Me Me Et 1 CF₂Cl —SO₂—(4-Me—Ph) 4-159 Me Me Me n-Pr 1 CF₂Cl —SO₂—(4-Me—Ph) 4-160 Me Me Me Me 2 CF₂Cl —SO₂—(4-Me—Ph) 4-161 Me Me Me Et 2 CF₂Cl —SO₂—(4-Me—Ph) 4-162 Me Me Me n-Pr 2 CF₂Cl —SO₂—(4-Me—Ph) 4-163 Me Me Me Me 0 CF₂Cl —SO₂-(Thien-2-yl) 4-164 Me Me Me Et 0 CF₂Cl —SO₂-(Thien-2-yl) 4-165 Me Me Me n-Pr 0 CF₂Cl —SO₂-(Thien-2-yl) 4-166 Me Me Me Me 1 CF₂Cl —SO₂-(Thien-2-yl) 4-167 Me Me Me Et 1 CF₂Cl —SO₂-(Thien-2-yl) 4-168 Me Me Me n-Pr 1 CF₂Cl —SO₂-(Thien-2-yl) 4-169 Me Me Me Me 2 CF₂Cl —SO₂-(Thien-2-yl) 4-170 Me Me Me Et 2 CF₂Cl —SO₂-(Thien-2-yl) 4-171 Me Me Me n-Pr 2 CF₂Cl —SO₂-(Thien-2-yl) 4-172 Me Me Me Me 0 CF₂Cl —CO—Ph 4-173 Me Me Me Et 0 CF₂Cl —CO—Ph 4-174 Me Me Me n-Pr 0 CF₂Cl —CO—Ph 4-175 Me Me Me Me 1 CF₂Cl —CO—Ph 4-176 Me Me Me Et 1 CF₂Cl —CO—Ph 4-177 Me Me Me n-Pr 1 CF₂Cl —CO—Ph 4-178 Me Me Me Me 2 CF₂Cl —CO—Ph 4-179 Me Me Me Et 2 CF₂Cl —CO—Ph 4-180 Me Me Me n-Pr 2 CF₂Cl —CO—Ph 4-181 Me Me Me Me 0 CF₂Cl —CH₂—CO—Ph 4-182 Me Me Me Et 0 CF₂Cl —CH₂—CO—Ph 4-183 Me Me Me n-Pr 0 CF₂Cl —CH₂—CO—Ph 4-184 Me Me Me Me 1 CF₂Cl —CH₂—CO—Ph 4-185 Me Me Me Et 1 CF₂Cl —CH₂—CO—Ph 4-186 Me Me Me n-Pr 1 CF₂Cl —CH₂—CO—Ph 4-187 Me Me Me Me 2 CF₂Cl —CH₂—CO—Ph 4-188 Me Me Me Et 2 CF₂Cl —CH₂—CO—Ph 4-189 Me Me Me n-Pr 2 CF₂Cl —CH₂—CO—Ph 4-190 Me H Me Me 0 CFCl₂ —SO₂—n-Pr 4-191 Me H Me Et 0 CFCl₂ —SO₂—n-Pr 4-192 Me H Me n-Pr 0 CFCl₂ —SO₂—n-Pr 4-193 Me H Me Me 1 CFCl₂ —SO₂—n-Pr 4-194 Me H Me Et 1 CFCl₂ —SO₂—n-Pr 4-195 Me H Me n-Pr 1 CFCl₂ —SO₂—n-Pr 4-196 Me H Me Me 2 CFCl₂ —SO₂—n-Pr 4-197 Me H Me Et 2 CFCl₂ —SO₂—n-Pr 4-198 Me H Me n-Pr 2 CFCl₂ —SO₂—n-Pr 4-199 Me H Me Me 0 CFCl₂ —SO₂—(CH₂)₂OMe 4-200 Me H Me Et 0 CFCl₂ —SO₂—(CH₂)₂OMe 4-201 Me H Me n-Pr 0 CFCl₂ —SO₂—(CH₂)₂OMe 4-202 Me H Me Me 1 CFCl₂ —SO₂—(CH₂)₂OMe 4-203 Me H Me Et 1 CFCl₂ —SO₂—(CH₂)₂OMe 4-204 Me H Me n-Pr 1 CFCl₂ —SO₂—(CH₂)₂OMe 4-205 Me H Me Me 2 CFCl₂ —SO₂—(CH₂)₂OMe 4-206 Me H Me Et 2 CFCl₂ —SO₂—(CH₂)₂OMe 4-207 Me H Me n-Pr 2 CFCl₂ —SO₂—(CH₂)₂OMe 4-208 Me H Me Me 0 CFCl₂ —SO₂—Ph 4-209 Me H Me Et 0 CFCl₂ —SO₂—Ph 4-210 Me H Me n-Pr 0 CFCl₂ —SO₂—Ph 4-211 Me H Me Me 1 CFCl₂ —SO₂—Ph 4-212 Me H Me Et 1 CFCl₂ —SO₂—Ph 4-213 Me H Me n-Pr 1 CFCl₂ —SO₂—Ph 4-214 Me H Me Me 2 CFCl₂ —SO₂—Ph 4-215 Me H Me Et 2 CFCl₂ —SO₂—Ph 4-216 Me H Me n-Pr 2 CFCl₂ —SO₂—Ph 4-217 Me H Me Me 0 CFCl₂ —SO₂—(4-Me—Ph) 4-218 Me H Me Et 0 CFCl₂ —SO₂—(4-Me—Ph) 4-219 Me H Me n-Pr 0 CFCl₂ —SO₂—(4-Me—Ph) 4-220 Me H Me Me 1 CFCl₂ —SO₂—(4-Me—Ph) 4-221 Me H Me Et 1 CFCl₂ —SO₂—(4-Me—Ph) 4-222 Me H Me n-Pr 1 CFCl₂ —SO₂—(4-Me—Ph) 4-223 Me H Me Me 2 CFCl₂ —SO₂—(4-Me—Ph) 4-224 Me H Me Et 2 CFCl₂ —SO₂—(4-Me—Ph) 4-225 Me H Me n-Pr 2 CFCl₂ —SO₂—(4-Me—Ph) 4-226 Me H Me Me 0 CFCl₂ —SO₂-(Thien-2-yl) 4-227 Me H Me Et 0 CFCl₂ —SO₂-(Thien-2-yl) 4-228 Me H Me n-Pr 0 CFCl₂ —SO₂-(Thien-2-yl) 4-229 Me H Me Me 1 CFCl₂ —SO₂-(Thien-2-yl) 4-230 Me H Me Et 1 CFCl₂ —SO₂-(Thien-2-yl) 4-231 Me H Me n-Pr 1 CFCl₂ —SO₂-(Thien-2-yl) 4-232 Me H Me Me 2 CFCl₂ —SO₂-(Thien-2-yl) 4-233 Me H Me Et 2 CFCl₂ —SO₂-(Thien-2-yl) 4-234 Me H Me n-Pr 2 CFCl₂ —SO₂-(Thien-2-yl) 4-235 Me H Me Me 0 CFCl₂ —CO—Ph 4-236 Me H Me Et 0 CFCl₂ —CO—Ph 4-237 Me H Me n-Pr 0 CFCl₂ —CO—Ph 4-238 Me H Me Me 1 CFCl₂ —CO—Ph 4-239 Me H Me Et 1 CFCl₂ —CO—Ph 4-240 Me H Me n-Pr 1 CFCl₂ —CO—Ph 4-241 Me H Me Me 2 CFCl₂ —CO—Ph 4-242 Me H Me Et 2 CFCl₂ —CO—Ph 4-243 Me H Me n-Pr 2 CFCl₂ —CO—Ph 4-244 Me H Me Me 0 CFCl₂ —CH₂—CO—Ph 4-245 Me H Me Et 0 CFCl₂ —CH₂—CO—Ph 4-246 Me H Me n-Pr 0 CFCl₂ —CH₂—CO—Ph 4-247 Me H Me Me 1 CFCl₂ —CH₂—CO—Ph 4-248 Me H Me Et 1 CFCl₂ —CH₂—CO—Ph 4-249 Me H Me n-Pr 1 CFCl₂ —CH₂—CO—Ph 4-250 Me H Me Me 2 CFCl₂ —CH₂—CO—Ph 4-251 Me H Me Et 2 CFCl₂ —CH₂—CO—Ph 4-252 Me H Me n-Pr 2 CFCl₂ —CH₂—CO—Ph 4-253 Et H Me Me 0 CFCl₂ —SO₂—n-Pr 4-254 Et H Me Et 0 CFCl₂ —SO₂—n-Pr 4-255 Et H Me n-Pr 0 CFCl₂ —SO₂—n-Pr 4-256 Et H Me Me 1 CFCl₂ —SO₂—n-Pr 4-257 Et H Me Et 1 CFCl₂ —SO₂—n-Pr 4-258 Et H Me n-Pr 1 CFCl₂ —SO₂—n-Pr 4-259 Et H Me Me 2 CFCl₂ —SO₂—n-Pr 4-260 Et H Me Et 2 CFCl₂ —SO₂—n-Pr 4-261 Et H Me n-Pr 2 CFCl₂ —SO₂—n-Pr 4-262 Et H Me Me 0 CFCl₂ —SO₂—(CH₂)₂OMe 4-263 Et H Me Et 0 CFCl₂ —SO₂—(CH₂)₂OMe 4-264 Et H Me n-Pr 0 CFCl₂ —SO₂—(CH₂)₂OMe 4-265 Et H Me Me 1 CFCl₂ —SO₂—(CH₂)₂OMe 4-266 Et H Me Et 1 CFCl₂ —SO₂—(CH₂)₂OMe 4-267 Et H Me n-Pr 1 CFCl₂ —SO₂—(CH₂)₂OMe 4-268 Et H Me Me 2 CFCl₂ —SO₂—(CH₂)₂OMe 4-269 Et H Me Et 2 CFCl₂ —SO₂—(CH₂)₂OMe 4-270 Et H Me n-Pr 2 CFCl₂ —SO₂—(CH₂)₂OMe 4-271 Et H Me Me 0 CFCl₂ —SO₂—Ph 4-272 Et H Me Et 0 CFCl₂ —SO₂—Ph 4-273 Et H Me n-Pr 0 CFCl₂ —SO₂—Ph 4-274 Et H Me Me 1 CFCl₂ —SO₂—Ph 4-275 Et H Me Et 1 CFCl₂ —SO₂—Ph 4-276 Et H Me n-Pr 1 CFCl₂ —SO₂—Ph 4-277 Et H Me Me 2 CFCl₂ —SO₂—Ph 4-278 Et H Me Et 2 CFCl₂ —SO₂—Ph 4-279 Et H Me n-Pr 2 CFCl₂ —SO₂—Ph 4-280 Et H Me Me 0 CFCl₂ —SO₂—(4-Me—Ph) 4-281 Et H Me Et 0 CFCl₂ —SO₂—(4-Me—Ph) 4-282 Et H Me n-Pr 0 CFCl₂ —SO₂—(4-Me—Ph) 4-283 Et H Me Me 1 CFCl₂ —SO₂—(4-Me—Ph) 4-284 Et H Me Et 1 CFCl₂ —SO₂—(4-Me—Ph) 4-285 Et H Me n-Pr 1 CFCl₂ —SO₂—(4-Me—Ph) 4-286 Et H Me Me 2 CFCl₂ —SO₂—(4-Me—Ph) 4-287 Et H Me Et 2 CFCl₂ —SO₂—(4-Me—Ph) 4-288 Et H Me n-Pr 2 CFCl₂ —SO₂—(4-Me—Ph) 4-289 Et H Me Me 0 CFCl₂ —SO₂-(Thien-2-yl) 4-290 Et H Me Et 0 CFCl₂ —SO₂-(Thien-2-yl) 4-291 Et H Me n-Pr 0 CFCl₂ —SO₂-(Thien-2-yl) 4-292 Et H Me Me 1 CFCl₂ —SO₂-(Thien-2-yl) 4-293 Et H Me Et 1 CFCl₂ —SO₂-(Thien-2-yl) 4-294 Et H Me n-Pr 1 CFCl₂ —SO₂-(Thien-2-yl) 4-295 Et H Me Me 2 CFCl₂ —SO₂-(Thien-2-yl) 4-296 Et H Me Et 2 CFCl₂ —SO₂-(Thien-2-yl) 4-297 Et H Me n-Pr 2 CFCl₂ —SO₂-(Thien-2-yl) 4-298 Et H Me Me 0 CFCl₂ —CO—Ph 4-299 Et H Me Et 0 CFCl₂ —CO—Ph 4-300 Et H Me n-Pr 0 CFCl₂ —CO—Ph 4-301 Et H Me Me 1 CFCl₂ —CO—Ph 4-302 Et H Me Et 1 CFCl₂ —CO—Ph 4-303 Et H Me n-Pr 1 CFCl₂ —CO—Ph 4-304 Et H Me Me 2 CFCl₂ —CO—Ph 4-305 Et H Me Et 2 CFCl₂ —CO—Ph 4-306 Et H Me n-Pr 2 CFCl₂ —CO—Ph 4-307 Et H Me Me 0 CFCl₂ —CH₂—CO—Ph 4-308 Et H Me Et 0 CFCl₂ —CH₂—CO—Ph 4-309 Et H Me n-Pr 0 CFCl₂ —CH₂—CO—Ph 4-310 Et H Me Me 1 CFCl₂ —CH₂—CO—Ph 4-311 Et H Me Et 1 CFCl₂ —CH₂—CO—Ph 4-312 Et H Me n-Pr 1 CFCl₂ —CH₂—CO—Ph 4-313 Et H Me Me 2 CFCl₂ —CH₂—CO—Ph 4-314 Et H Me Et 2 CFCl₂ —CH₂—CO—Ph 4-315 Et H Me n-Pr 2 CFCl₂ —CH₂—CO—Ph 4-316 Me Me Me Me 0 CFCl₂ —SO₂—n-Pr 4-317 Me Me Me Et 0 CFCl₂ —SO₂—n-Pr 4-318 Me Me Me n-Pr 0 CFCl₂ —SO₂—n-Pr 4-319 Me Me Me Me 1 CFCl₂ —SO₂—n-Pr 4-320 Me Me Me Et 1 CFCl₂ —SO₂—n-Pr 4-321 Me Me Me n-Pr 1 CFCl₂ —SO₂—n-Pr 4-322 Me Me Me Me 2 CFCl₂ —SO₂—n-Pr 4-323 Me Me Me Et 2 CFCl₂ —SO₂—n-Pr 4-324 Me Me Me n-Pr 2 CFCl₂ —SO₂—n-Pr 4-325 Me Me Me Me 0 CFCl₂ —SO₂—(CH₂)₂OMe 4-326 Me Me Me Et 0 CFCl₂ —SO₂—(CH₂)₂OMe 4-327 Me Me Me n-Pr 0 CFCl₂ —SO₂—(CH₂)₂OMe 4-328 Me Me Me Me 1 CFCl₂ —SO₂—(CH₂)₂OMe 4-329 Me Me Me Et 1 CFCl₂ —SO₂—(CH₂)₂OMe 4-330 Me Me Me n-Pr 1 CFCl₂ —SO₂—(CH₂)₂OMe 4-331 Me Me Me Me 2 CFCl₂ —SO₂—(CH₂)₂OMe 4-332 Me Me Me Et 2 CFCl₂ —SO₂—(CH₂)₂OMe 4-333 Me Me Me n-Pr 2 CFCl₂ —SO₂—(CH₂)₂OMe 4-334 Me Me Me Me 0 CFCl₂ —SO₂—Ph 4-335 Me Me Me Et 0 CFCl₂ —SO₂—Ph 4-336 Me Me Me n-Pr 0 CFCl₂ —SO₂—Ph 4-337 Me Me Me Me 1 CFCl₂ —SO₂—Ph 4-338 Me Me Me Et 1 CFCl₂ —SO₂—Ph 4-339 Me Me Me n-Pr 1 CFCl₂ —SO₂—Ph 4-340 Me Me Me Me 2 CFCl₂ —SO₂—Ph 4-341 Me Me Me Et 2 CFCl₂ —SO₂—Ph 4-342 Me Me Me n-Pr 2 CFCl₂ —SO₂—Ph 4-343 Me Me Me Me 0 CFCl₂ —SO₂—(4-Me—Ph) 4-344 Me Me Me Et 0 CFCl₂ —SO₂—(4-Me—Ph) 4-345 Me Me Me n-Pr 0 CFCl₂ —SO₂—(4-Me—Ph) 4-346 Me Me Me Me 1 CFCl₂ —SO₂—(4-Me—Ph) 4-347 Me Me Me Et 1 CFCl₂ —SO₂—(4-Me—Ph) 4-348 Me Me Me n-Pr 1 CFCl₂ —SO₂—(4-Me—Ph) 4-349 Me Me Me Me 2 CFCl₂ —SO₂—(4-Me—Ph) 4-350 Me Me Me Et 2 CFCl₂ —SO₂—(4-Me—Ph) 4-351 Me Me Me n-Pr 2 CFCl₂ —SO₂—(4-Me—Ph) 4-352 Me Me Me Me 0 CFCl₂ —SO₂-(Thien-2-yl) 4-353 Me Me Me Et 0 CFCl₂ —SO₂-(Thien-2-yl) 4-354 Me Me Me n-Pr 0 CFCl₂ —SO₂-(Thien-2-yl) 4-355 Me Me Me Me 1 CFCl₂ —SO₂-(Thien-2-yl) 4-356 Me Me Me Et 1 CFCl₂ —SO₂-(Thien-2-yl) 4-357 Me Me Me n-Pr 1 CFCl₂ —SO₂-(Thien-2-yl) 4-358 Me Me Me Me 2 CFCl₂ —SO₂-(Thien-2-yl) 4-359 Me Me Me Et 2 CFCl₂ —SO₂-(Thien-2-yl) 4-360 Me Me Me n-Pr 2 CFCl₂ —SO₂-(Thien-2-yl) 4-361 Me Me Me Me 0 CFCl₂ —CO—Ph 4-362 Me Me Me Et 0 CFCl₂ —CO—Ph 4-363 Me Me Me n-Pr 0 CFCl₂ —CO—Ph 4-364 Me Me Me Me 1 CFCl₂ —CO—Ph 4-365 Me Me Me Et 1 CFCl₂ —CO—Ph 4-366 Me Me Me n-Pr 1 CFCl₂ —CO—Ph 4-367 Me Me Me Me 2 CFCl₂ —CO—Ph 4-368 Me Me Me Et 2 CFCl₂ —CO—Ph 4-369 Me Me Me n-Pr 2 CFCl₂ —CO—Ph 4-370 Me Me Me Me 0 CFCl₂ —CH₂—CO—Ph 4-371 Me Me Me Et 0 CFCl₂ —CH₂—CO—Ph 4-372 Me Me Me n-Pr 0 CFCl₂ —CH₂—CO—Ph 4-373 Me Me Me Me 1 CFCl₂ —CH₂—CO—Ph 4-374 Me Me Me Et 1 CFCl₂ —CH₂—CO—Ph 4-375 Me Me Me n-Pr 1 CFCl₂ —CH₂—CO—Ph 4-376 Me Me Me Me 2 CFCl₂ —CH₂—CO—Ph 4-377 Me Me Me Et 2 CFCl₂ —CH₂—CO—Ph 4-378 Me Me Me n-Pr 2 CFCl₂ —CH₂—CO—Ph 4-379 Me H Me Me 0 CCl₃ —SO₂—n-Pr 4-380 Me H Me Et 0 CCl₃ —SO₂—n-Pr 4-381 Me H Me n-Pr 0 CCl₃ —SO₂—n-Pr 4-382 Me H Me Me 1 CCl₃ —SO₂—n-Pr 4-383 Me H Me Et 1 CCl₃ —SO₂—n-Pr 4-384 Me H Me n-Pr 1 CCl₃ —SO₂—n-Pr 4-385 Me H Me Me 2 CCl₃ —SO₂—n-Pr 4-386 Me H Me Et 2 CCl₃ —SO₂—n-Pr 4-387 Me H Me n-Pr 2 CCl₃ —SO₂—n-Pr 4-388 Me H Me Me 0 CCl₃ —SO₂—(CH₂)₂OMe 4-389 Me H Me Et 0 CCl₃ —SO₂—(CH₂)₂OMe 4-390 Me H Me n-Pr 0 CCl₃ —SO₂—(CH₂)₂OMe 4-391 Me H Me Me 1 CCl₃ —SO₂—(CH₂)₂OMe 4-392 Me H Me Et 1 CCl₃ —SO₂—(CH₂)₂OMe 4-393 Me H Me n-Pr 1 CCl₃ —SO₂—(CH₂)₂OMe 4-394 Me H Me Me 2 CCl₃ —SO₂—(CH₂)₂OMe 4-395 Me H Me Et 2 CCl₃ —SO₂—(CH₂)₂OMe 4-396 Me H Me n-Pr 2 CCl₃ —SO₂—(CH₂)₂OMe 4-397 Me H Me Me 0 CCl₃ —SO₂—Ph 4-398 Me H Me Et 0 CCl₃ —SO₂—Ph 4-399 Me H Me n-Pr 0 CCl₃ —SO₂—Ph 4-400 Me H Me Me 1 CCl₃ —SO₂—Ph 4-401 Me H Me Et 1 CCl₃ —SO₂—Ph 4-402 Me H Me n-Pr 1 CCl₃ —SO₂—Ph 4-403 Me H Me Me 2 CCl₃ —SO₂—Ph 4-404 Me H Me Et 2 CCl₃ —SO₂—Ph 4-405 Me H Me n-Pr 2 CCl₃ —SO₂—Ph 4-406 Me H Me Me 0 CCl₃ —SO₂—(4-Me—Ph) 4-407 Me H Me Et 0 CCl₃ —SO₂—(4-Me—Ph) 4-408 Me H Me n-Pr 0 CCl₃ —SO₂—(4-Me—Ph) 4-409 Me H Me Me 1 CCl₃ —SO₂—(4-Me—Ph) 4-410 Me H Me Et 1 CCl₃ —SO₂—(4-Me—Ph) 4-411 Me H Me n-Pr 1 CCl₃ —SO₂—(4-Me—Ph) 4-412 Me H Me Me 2 CCl₃ —SO₂—(4-Me—Ph) 4-413 Me H Me Et 2 CCl₃ —SO₂—(4-Me—Ph) 4-414 Me H Me n-Pr 2 CCl₃ —SO₂—(4-Me—Ph) 4-415 Me H Me Me 0 CCl₃ —SO₂-(Thien-2-yl) 4-416 Me H Me Et 0 CCl₃ —SO₂-(Thien-2-yl) 4-417 Me H Me n-Pr 0 CCl₃ —SO₂-(Thien-2-yl) 4-418 Me H Me Me 1 CCl₃ —SO₂-(Thien-2-yl) 4-419 Me H Me Et 1 CCl₃ —SO₂-(Thien-2-yl) 4-420 Me H Me n-Pr 1 CCl₃ —SO₂-(Thien-2-yl) 4-421 Me H Me Me 2 CCl₃ —SO₂-(Thien-2-yl) 4-422 Me H Me Et 2 CCl₃ —SO₂-(Thien-2-yl) 4-423 Me H Me n-Pr 2 CCl₃ —SO₂-(Thien-2-yl) 4-424 Me H Me Me 0 CCl₃ —CO—Ph 4-425 Me H Me Et 0 CCl₃ —CO—Ph 4-426 Me H Me n-Pr 0 CCl₃ —CO—Ph 4-427 Me H Me Me 1 CCl₃ —CO—Ph 4-428 Me H Me Et 1 CCl₃ —CO—Ph 4-429 Me H Me n-Pr 1 CCl₃ —CO—Ph 4-430 Me H Me Me 2 CCl₃ —CO—Ph 4-431 Me H Me Et 2 CCl₃ —CO—Ph 4-432 Me H Me n-Pr 2 CCl₃ —CO—Ph 4-433 Me H Me Me 0 CCl₃ —CH₂—CO—Ph 4-434 Me H Me Et 0 CCl₃ —CH₂—CO—Ph 4-435 Me H Me n-Pr 0 CCl₃ —CH₂—CO—Ph 4-436 Me H Me Me 1 CCl₃ —CH₂—CO—Ph 4-437 Me H Me Et 1 CCl₃ —CH₂—CO—Ph 4-438 Me H Me n-Pr 1 CCl₃ —CH₂—CO—Ph 4-439 Me H Me Me 2 CCl₃ —CH₂—CO—Ph 4-440 Me H Me Et 2 CCl₃ —CH₂—CO—Ph 4-441 Me H Me n-Pr 2 CCl₃ —CH₂—CO—Ph 4-442 Et H Me Me 0 CCl₃ —SO₂—n-Pr 4-443 Et H Me Et 0 CCl₃ —SO₂—n-Pr 4-444 Et H Me n-Pr 0 CCl₃ —SO₂—n-Pr 4-445 Et H Me Me 1 CCl₃ —SO₂—n-Pr 4-446 Et H Me Et 1 CCl₃ —SO₂—n-Pr 4-447 Et H Me n-Pr 1 CCl₃ —SO₂—n-Pr 4-448 Et H Me Me 2 CCl₃ —SO₂—n-Pr 4-449 Et H Me Et 2 CCl₃ —SO₂—n-Pr 4-450 Et H Me n-Pr 2 CCl₃ —SO₂—n-Pr 4-451 Et H Me Me 0 CCl₃ —SO₂—(CH₂)₂OMe 4-452 Et H Me Et 0 CCl₃ —SO₂—(CH₂)₂OMe 4-453 Et H Me n-Pr 0 CCl₃ —SO₂—(CH₂)₂OMe 4-454 Et H Me Me 1 CCl₃ —SO₂—(CH₂)₂OMe 4-455 Et H Me Et 1 CCl₃ —SO₂—(CH₂)₂OMe 4-456 Et H Me n-Pr 1 CCl₃ —SO₂—(CH₂)₂OMe 4-457 Et H Me Me 2 CCl₃ —SO₂—(CH₂)₂OMe 4-458 Et H Me Et 2 CCl₃ —SO₂—(CH₂)₂OMe 4-459 Et H Me n-Pr 2 CCl₃ —SO₂—(CH₂)₂OMe 4-460 Et H Me Me 0 CCl₃ —SO₂—Ph 4-461 Et H Me Et 0 CCl₃ —SO₂—Ph 4-462 Et H Me n-Pr 0 CCl₃ —SO₂—Ph 4-463 Et H Me Me 1 CCl₃ —SO₂—Ph 4-464 Et H Me Et 1 CCl₃ —SO₂—Ph 4-465 Et H Me n-Pr 1 CCl₃ —SO₂—Ph 4-466 Et H Me Me 2 CCl₃ —SO₂—Ph 4-467 Et H Me Et 2 CCl₃ —SO₂—Ph 4-468 Et H Me n-Pr 2 CCl₃ —SO₂—Ph 4-469 Et H Me Me 0 CCl₃ —SO₂—(4-Me—Ph) 4-470 Et H Me Et 0 CCl₃ —SO₂—(4-Me—Ph) 4-471 Et H Me n-Pr 0 CCl₃ —SO₂—(4-Me—Ph) 4-472 Et H Me Me 1 CCl₃ —SO₂—(4-Me—Ph) 4-473 Et H Me Et 1 CCl₃ —SO₂—(4-Me—Ph) 4-474 Et H Me n-Pr 1 CCl₃ —SO₂—(4-Me—Ph) 4-475 Et H Me Me 2 CCl₃ —SO₂—(4-Me—Ph) 4-476 Et H Me Et 2 CCl₃ —SO₂—(4-Me—Ph) 4-477 Et H Me n-Pr 2 CCl₃ —SO₂—(4-Me—Ph) 4-478 Et H Me Me 0 CCl₃ —SO₂-(Thien-2-yl) 4-479 Et H Me Et 0 CCl₃ —SO₂-(Thien-2-yl) 4-480 Et H Me n-Pr 0 CCl₃ —SO₂-(Thien-2-yl) 4-481 Et H Me Me 1 CCl₃ —SO₂-(Thien-2-yl) 4-482 Et H Me Et 1 CCl₃ —SO₂-(Thien-2-yl) 4-483 Et H Me n-Pr 1 CCl₃ —SO₂-(Thien-2-yl) 4-484 Et H Me Me 2 CCl₃ —SO₂-(Thien-2-yl) 4-485 Et H Me Et 2 CCl₃ —SO₂-(Thien-2-yl) 4-486 Et H Me n-Pr 2 CCl₃ —SO₂-(Thien-2-yl) 4-487 Et H Me Me 0 CCl₃ —CO—Ph 4-488 Et H Me Et 0 CCl₃ —CO—Ph 4-489 Et H Me n-Pr 0 CCl₃ —CO—Ph 4-490 Et H Me Me 1 CCl₃ —CO—Ph 4-491 Et H Me Et 1 CCl₃ —CO—Ph 4-492 Et H Me n-Pr 1 CCl₃ —CO—Ph 4-493 Et H Me Me 2 CCl₃ —CO—Ph 4-494 Et H Me Et 2 CCl₃ —CO—Ph 4-495 Et H Me n-Pr 2 CCl₃ —CO—Ph 4-496 Et H Me Me 0 CCl₃ —CH₂—CO—Ph 4-497 Et H Me Et 0 CCl₃ —CH₂—CO—Ph 4-498 Et H Me n-Pr 0 CCl₃ —CH₂—CO—Ph 4-499 Et H Me Me 1 CCl₃ —CH₂—CO—Ph 4-500 Et H Me Et 1 CCl₃ —CH₂—CO—Ph 4-501 Et H Me n-Pr 1 CCl₃ —CH₂—CO—Ph 4-502 Et H Me Me 2 CCl₃ —CH₂—CO—Ph 4-503 Et H Me Et 2 CCl₃ —CH₂—CO—Ph 4-504 Et H Me n-Pr 2 CCl₃ —CH₂—CO—Ph 4-505 Me Me Me Me 0 CCl₃ —SO₂—n-Pr 4-506 Me Me Me Et 0 CCl₃ —SO₂—n-Pr 4-507 Me Me Me n-Pr 0 CCl₃ —SO₂—n-Pr 4-508 Me Me Me Me 1 CCl₃ —SO₂—n-Pr 4-509 Me Me Me Et 1 CCl₃ —SO₂—n-Pr 4-510 Me Me Me n-Pr 1 CCl₃ —SO₂—n-Pr 4-511 Me Me Me Me 2 CCl₃ —SO₂—n-Pr 4-512 Me Me Me Et 2 CCl₃ —SO₂—n-Pr 4-513 Me Me Me n-Pr 2 CCl₃ —SO₂—n-Pr 4-514 Me Me Me Me 0 CCl₃ —SO₂—(CH₂)₂OMe 4-515 Me Me Me Et 0 CCl₃ —SO₂—(CH₂)₂OMe 4-516 Me Me Me n-Pr 0 CCl₃ —SO₂—(CH₂)₂OMe 4-517 Me Me Me Me 1 CCl₃ —SO₂—(CH₂)₂OMe 4-518 Me Me Me Et 1 CCl₃ —SO₂—(CH₂)₂OMe 4-519 Me Me Me n-Pr 1 CCl₃ —SO₂—(CH₂)₂OMe 4-520 Me Me Me Me 2 CCl₃ —SO₂—(CH₂)₂OMe 4-521 Me Me Me Et 2 CCl₃ —SO₂—(CH₂)₂OMe 4-522 Me Me Me n-Pr 2 CCl₃ —SO₂—(CH₂)₂OMe 4-523 Me Me Me Me 0 CCl₃ —SO₂—Ph 4-524 Me Me Me Et 0 CCl₃ —SO₂—Ph 4-525 Me Me Me n-Pr 0 CCl₃ —SO₂—Ph 4-526 Me Me Me Me 1 CCl₃ —SO₂—Ph 4-527 Me Me Me Et 1 CCl₃ —SO₂—Ph 4-528 Me Me Me n-Pr 1 CCl₃ —SO₂—Ph 4-529 Me Me Me Me 2 CCl₃ —SO₂—Ph 4-530 Me Me Me Et 2 CCl₃ —SO₂—Ph 4-531 Me Me Me n-Pr 2 CCl₃ —SO₂—Ph 4-532 Me Me Me Me 0 CCl₃ —SO₂—(4-Me—Ph) 4-533 Me Me Me Et 0 CCl₃ —SO₂—(4-Me—Ph) 4-534 Me Me Me n-Pr 0 CCl₃ —SO₂—(4-Me—Ph) 4-535 Me Me Me Me 1 CCl₃ —SO₂—(4-Me—Ph) 4-536 Me Me Me Et 1 CCl₃ —SO₂—(4-Me—Ph) 4-537 Me Me Me n-Pr 1 CCl₃ —SO₂—(4-Me—Ph) 4-538 Me Me Me Me 2 CCl₃ —SO₂—(4-Me—Ph) 4-539 Me Me Me Et 2 CCl₃ —SO₂—(4-Me—Ph) 4-540 Me Me Me n-Pr 2 CCl₃ —SO₂—(4-Me—Ph) 4-541 Me Me Me Me 0 CCl₃ —SO₂-(Thien-2-yl) 4-542 Me Me Me Et 0 CCl₃ —SO₂-(Thien-2-yl) 4-543 Me Me Me n-Pr 0 CCl₃ —SO₂-(Thien-2-yl) 4-544 Me Me Me Me 1 CCl₃ —SO₂-(Thien-2-yl) 4-545 Me Me Me Et 1 CCl₃ —SO₂-(Thien-2-yl) 4-546 Me Me Me n-Pr 1 CCl₃ —SO₂-(Thien-2-yl) 4-547 Me Me Me Me 2 CCl₃ —SO₂-(Thien-2-yl) 4-548 Me Me Me Et 2 CCl₃ —SO₂-(Thien-2-yl) 4-549 Me Me Me n-Pr 2 CCl₃ —SO₂-(Thien-2-yl) 4-550 Me Me Me Me 0 CCl₃ —CO—Ph 4-551 Me Me Me Et 0 CCl₃ —CO—Ph 4-552 Me Me Me n-Pr 0 CCl₃ —CO—Ph 4-553 Me Me Me Me 1 CCl₃ —CO—Ph 4-554 Me Me Me Et 1 CCl₃ —CO—Ph 4-555 Me Me Me n-Pr 1 CCl₃ —CO—Ph 4-556 Me Me Me Me 2 CCl₃ —CO—Ph 4-557 Me Me Me Et 2 CCl₃ —CO—Ph 4-558 Me Me Me n-Pr 2 CCl₃ —CO—Ph 4-559 Me Me Me Me 0 CCl₃ —CH₂—CO—Ph 4-560 Me Me Me Et 0 CCl₃ —CH₂—CO—Ph 4-561 Me Me Me n-Pr 0 CCl₃ —CH₂—CO—Ph 4-562 Me Me Me Me 1 CCl₃ —CH₂—CO—Ph 4-563 Me Me Me Et 1 CCl₃ —CH₂—CO—Ph 4-564 Me Me Me n-Pr 1 CCl₃ —CH₂—CO—Ph 4-565 Me Me Me Me 2 CCl₃ —CH₂—CO—Ph 4-566 Me Me Me Et 2 CCl₃ —CH₂—CO—Ph 4-567 Me Me Me n-Pr 2 CCl₃ —CH₂—CO—Ph 4-568 Me H Me Me 0 C₂F₅ —SO₂—n-Pr 4-569 Me H Me Et 0 C₂F₅ —SO₂—n-Pr 4-570 Me H Me n-Pr 0 C₂F₅ —SO₂—n-Pr 4-571 Me H Me Me 1 C₂F₅ —SO₂—n-Pr 4-572 Me H Me Et 1 C₂F₅ —SO₂—n-Pr 4-573 Me H Me n-Pr 1 C₂F₅ —SO₂—n-Pr 4-574 Me H Me Me 2 C₂F₅ —SO₂—n-Pr 4-575 Me H Me Et 2 C₂F₅ —SO₂—n-Pr 4-576 Me H Me n-Pr 2 C₂F₅ —SO₂—n-Pr 4-577 Me H Me Me 0 C₂F₅ —SO₂—(CH₂)₂OMe 4-578 Me H Me Et 0 C₂F₅ —SO₂—(CH₂)₂OMe 4-579 Me H Me n-Pr 0 C₂F₅ —SO₂—(CH₂)₂OMe 4-580 Me H Me Me 1 C₂F₅ —SO₂—(CH₂)₂OMe 4-581 Me H Me Et 1 C₂F₅ —SO₂—(CH₂)₂OMe 4-582 Me H Me n-Pr 1 C₂F₅ —SO₂—(CH₂)₂OMe 4-583 Me H Me Me 2 C₂F₅ —SO₂—(CH₂)₂OMe 4-584 Me H Me Et 2 C₂F₅ —SO₂—(CH₂)₂OMe 4-585 Me H Me n-Pr 2 C₂F₅ —SO₂—(CH₂)₂OMe 4-586 Me H Me Me 0 C₂F₅ —SO₂—Ph 4-587 Me H Me Et 0 C₂F₅ —SO₂—Ph 4-588 Me H Me n-Pr 0 C₂F₅ —SO₂—Ph 4-589 Me H Me Me 1 C₂F₅ —SO₂—Ph 4-590 Me H Me Et 1 C₂F₅ —SO₂—Ph 4-591 Me H Me n-Pr 1 C₂F₅ —SO₂—Ph 4-592 Me H Me Me 2 C₂F₅ —SO₂—Ph 4-593 Me H Me Et 2 C₂F₅ —SO₂—Ph 4-594 Me H Me n-Pr 2 C₂F₅ —SO₂—Ph 4-595 Me H Me Me 0 C₂F₅ —SO₂—(4-Me—Ph) 4-596 Me H Me Et 0 C₂F₅ —SO₂—(4-Me—Ph) 4-597 Me H Me n-Pr 0 C₂F₅ —SO₂—(4-Me—Ph) 4-598 Me H Me Me 1 C₂F₅ —SO₂—(4-Me—Ph) 4-599 Me H Me Et 1 C₂F₅ —SO₂—(4-Me—Ph) 4-600 Me H Me n-Pr 1 C₂F₅ —SO₂—(4-Me—Ph) 4-601 Me H Me Me 2 C₂F₅ —SO₂—(4-Me—Ph) 4-602 Me H Me Et 2 C₂F₅ —SO₂—(4-Me—Ph) 4-603 Me H Me n-Pr 2 C₂F₅ —SO₂—(4-Me—Ph) 4-604 Me H Me Me 0 C₂F₅ —SO₂-(Thien-2-yl) 4-605 Me H Me Et 0 C₂F₅ —SO₂-(Thien-2-yl) 4-606 Me H Me n-Pr 0 C₂F₅ —SO₂-(Thien-2-yl) 4-607 Me H Me Me 1 C₂F₅ —SO₂-(Thien-2-yl) 4-608 Me H Me Et 1 C₂F₅ —SO₂-(Thien-2-yl) 4-609 Me H Me n-Pr 1 C₂F₅ —SO₂-(Thien-2-yl) 4-610 Me H Me Me 2 C₂F₅ —SO₂-(Thien-2-yl) 4-611 Me H Me Et 2 C₂F₅ —SO₂-(Thien-2-yl) 4-612 Me H Me n-Pr 2 C₂F₅ —SO₂-(Thien-2-yl) 4-613 Me H Me Me 0 C₂F₅ —CO—Ph 4-614 Me H Me Et 0 C₂F₅ —CO—Ph 4-615 Me H Me n-Pr 0 C₂F₅ —CO—Ph 4-616 Me H Me Me 1 C₂F₅ —CO—Ph 4-617 Me H Me Et 1 C₂F₅ —CO—Ph 4-618 Me H Me n-Pr 1 C₂F₅ —CO—Ph 4-619 Me H Me Me 2 C₂F₅ —CO—Ph 4-620 Me H Me Et 2 C₂F₅ —CO—Ph 4-621 Me H Me n-Pr 2 C₂F₅ —CO—Ph 4-622 Me H Me Me 0 C₂F₅ —CH₂—CO—Ph 4-623 Me H Me Et 0 C₂F₅ —CH₂—CO—Ph 4-624 Me H Me n-Pr 0 C₂F₅ —CH₂—CO—Ph 4-625 Me H Me Me 1 C₂F₅ —CH₂—CO—Ph 4-626 Me H Me Et 1 C₂F₅ —CH₂—CO—Ph 4-627 Me H Me n-Pr 1 C₂F₅ —CH₂—CO—Ph 4-628 Me H Me Me 2 C₂F₅ —CH₂—CO—Ph 4-629 Me H Me Et 2 C₂F₅ —CH₂—CO—Ph 4-630 Me H Me n-Pr 2 C₂F₅ —CH₂—CO—Ph 4-631 Et H Me Me 0 C₂F₅ —SO₂—n-Pr 4-632 Et H Me Et 0 C₂F₅ —SO₂—n-Pr 4-633 Et H Me n-Pr 0 C₂F₅ —SO₂—n-Pr 4-634 Et H Me Me 1 C₂F₅ —SO₂—n-Pr 4-635 Et H Me Et 1 C₂F₅ —SO₂—n-Pr 4-636 Et H Me n-Pr 1 C₂F₅ —SO₂—n-Pr 4-637 Et H Me Me 2 C₂F₅ —SO₂—n-Pr 4-638 Et H Me Et 2 C₂F₅ —SO₂—n-Pr 4-639 Et H Me n-Pr 2 C₂F₅ —SO₂—n-Pr 4-640 Et H Me Me 0 C₂F₅ —SO₂—(CH₂)₂OMe 4-641 Et H Me Et 0 C₂F₅ —SO₂—(CH₂)₂OMe 4-642 Et H Me n-Pr 0 C₂F₅ —SO₂—(CH₂)₂OMe 4-643 Et H Me Me 1 C₂F₅ —SO₂—(CH₂)₂OMe 4-644 Et H Me Et 1 C₂F₅ —SO₂—(CH₂)₂OMe 4-645 Et H Me n-Pr 1 C₂F₅ —SO₂—(CH₂)₂OMe 4-646 Et H Me Me 2 C₂F₅ —SO₂—(CH₂)₂OMe 4-647 Et H Me Et 2 C₂F₅ —SO₂—(CH₂)₂OMe 4-648 Et H Me n-Pr 2 C₂F₅ —SO₂—(CH₂)₂OMe 4-649 Et H Me Me 0 C₂F₅ —SO₂—Ph 4-650 Et H Me Et 0 C₂F₅ —SO₂—Ph 4-651 Et H Me n-Pr 0 C₂F₅ —SO₂—Ph 4-652 Et H Me Me 1 C₂F₅ —SO₂—Ph 4-653 Et H Me Et 1 C₂F₅ —SO₂—Ph 4-654 Et H Me n-Pr 1 C₂F₅ —SO₂—Ph 4-655 Et H Me Me 2 C₂F₅ —SO₂—Ph 4-656 Et H Me Et 2 C₂F₅ —SO₂—Ph 4-657 Et H Me n-Pr 2 C₂F₅ —SO₂—Ph 4-658 Et H Me Me 0 C₂F₅ —SO₂—(4-Me—Ph) 4-659 Et H Me Et 0 C₂F₅ —SO₂—(4-Me—Ph) 4-660 Et H Me n-Pr 0 C₂F₅ —SO₂—(4-Me—Ph) 4-661 Et H Me Me 1 C₂F₅ —SO₂—(4-Me—Ph) 4-662 Et H Me Et 1 C₂F₅ —SO₂—(4-Me—Ph) 4-663 Et H Me n-Pr 1 C₂F₅ —SO₂—(4-Me—Ph) 4-664 Et H Me Me 2 C₂F₅ —SO₂—(4-Me—Ph) 4-665 Et H Me Et 2 C₂F₅ —SO₂—(4-Me—Ph) 4-666 Et H Me n-Pr 2 C₂F₅ —SO₂—(4-Me—Ph) 4-667 Et H Me Me 0 C₂F₅ —SO₂-(Thien-2-yl) 4-668 Et H Me Et 0 C₂F₅ —SO₂-(Thien-2-yl) 4-669 Et H Me n-Pr 0 C₂F₅ —SO₂-(Thien-2-yl) 4-670 Et H Me Me 1 C₂F₅ —SO₂-(Thien-2-yl) 4-671 Et H Me Et 1 C₂F₅ —SO₂-(Thien-2-yl) 4-672 Et H Me n-Pr 1 C₂F₅ —SO₂-(Thien-2-yl) 4-673 Et H Me Me 2 C₂F₅ —SO₂-(Thien-2-yl) 4-674 Et H Me Et 2 C₂F₅ —SO₂-(Thien-2-yl) 4-675 Et H Me n-Pr 2 C₂F₅ —SO₂-(Thien-2-yl) 4-676 Et H Me Me 0 C₂F₅ —CO—Ph 4-677 Et H Me Et 0 C₂F₅ —CO—Ph 4-678 Et H Me n-Pr 0 C₂F₅ —CO—Ph 4-679 Et H Me Me 1 C₂F₅ —CO—Ph 4-680 Et H Me Et 1 C₂F₅ —CO—Ph 4-681 Et H Me n-Pr 1 C₂F₅ —CO—Ph 4-682 Et H Me Me 2 C₂F₅ —CO—Ph 4-683 Et H Me Et 2 C₂F₅ —CO—Ph 4-684 Et H Me n-Pr 2 C₂F₅ —CO—Ph 4-685 Et H Me Me 0 C₂F₅ —CH₂—CO—Ph 4-686 Et H Me Et 0 C₂F₅ —CH₂—CO—Ph 4-687 Et H Me n-Pr 0 C₂F₅ —CH₂—CO—Ph 4-688 Et H Me Me 1 C₂F₅ —CH₂—CO—Ph 4-689 Et H Me Et 1 C₂F₅ —CH₂—CO—Ph 4-690 Et H Me n-Pr 1 C₂F₅ —CH₂—CO—Ph 4-691 Et H Me Me 2 C₂F₅ —CH₂—CO—Ph 4-692 Et H Me Et 2 C₂F₅ —CH₂—CO—Ph 4-693 Et H Me n-Pr 2 C₂F₅ —CH₂—CO—Ph 4-694 Me Me Me Me 0 C₂F₅ —SO₂—n-Pr 4-695 Me Me Me Et 0 C₂F₅ —SO₂—n-Pr 4-696 Me Me Me n-Pr 0 C₂F₅ —SO₂—n-Pr 4-697 Me Me Me Me 1 C₂F₅ —SO₂—n-Pr 4-698 Me Me Me Et 1 C₂F₅ —SO₂—n-Pr 4-699 Me Me Me n-Pr 1 C₂F₅ —SO₂—n-Pr 4-700 Me Me Me Me 2 C₂F₅ —SO₂—n-Pr 4-701 Me Me Me Et 2 C₂F₅ —SO₂—n-Pr 4-702 Me Me Me n-Pr 2 C₂F₅ —SO₂—n-Pr 4-703 Me Me Me Me 0 C₂F₅ —SO₂—(CH₂)₂OMe 4-704 Me Me Me Et 0 C₂F₅ —SO₂—(CH₂)₂OMe 4-705 Me Me Me n-Pr 0 C₂F₅ —SO₂—(CH₂)₂OMe 4-706 Me Me Me Me 1 C₂F₅ —SO₂—(CH₂)₂OMe 4-707 Me Me Me Et 1 C₂F₅ —SO₂—(CH₂)₂OMe 4-708 Me Me Me n-Pr 1 C₂F₅ —SO₂—(CH₂)₂OMe 4-709 Me Me Me Me 2 C₂F₅ —SO₂—(CH₂)₂OMe 4-710 Me Me Me Et 2 C₂F₅ —SO₂—(CH₂)₂OMe 4-711 Me Me Me n-Pr 2 C₂F₅ —SO₂—(CH₂)₂OMe 4-712 Me Me Me Me 0 C₂F₅ —SO₂—Ph 4-713 Me Me Me Et 0 C₂F₅ —SO₂—Ph 4-714 Me Me Me n-Pr 0 C₂F₅ —SO₂—Ph 4-715 Me Me Me Me 1 C₂F₅ —SO₂—Ph 4-716 Me Me Me Et 1 C₂F₅ —SO₂—Ph 4-717 Me Me Me n-Pr 1 C₂F₅ —SO₂—Ph 4-718 Me Me Me Me 2 C₂F₅ —SO₂—Ph 4-719 Me Me Me Et 2 C₂F₅ —SO₂—Ph 4-720 Me Me Me n-Pr 2 C₂F₅ —SO₂—Ph 4-721 Me Me Me Me 0 C₂F₅ —SO₂—(4-Me—Ph) 4-722 Me Me Me Et 0 C₂F₅ —SO₂—(4-Me—Ph) 4-723 Me Me Me n-Pr 0 C₂F₅ —SO₂—(4-Me—Ph) 4-724 Me Me Me Me 1 C₂F₅ —SO₂—(4-Me—Ph) 4-725 Me Me Me Et 1 C₂F₅ —SO₂—(4-Me—Ph) 4-726 Me Me Me n-Pr 1 C₂F₅ —SO₂—(4-Me—Ph) 4-727 Me Me Me Me 2 C₂F₅ —SO₂—(4-Me—Ph) 4-728 Me Me Me Et 2 C₂F₅ —SO₂—(4-Me—Ph) 4-729 Me Me Me n-Pr 2 C₂F₅ —SO₂—(4-Me—Ph) 4-730 Me Me Me Me 0 C₂F₅ —SO₂-(Thien-2-yl) 4-731 Me Me Me Et 0 C₂F₅ —SO₂-(Thien-2-yl) 4-732 Me Me Me n-Pr 0 C₂F₅ —SO₂-(Thien-2-yl) 4-733 Me Me Me Me 1 C₂F₅ —SO₂-(Thien-2-yl) 4-734 Me Me Me Et 1 C₂F₅ —SO₂-(Thien-2-yl) 4-735 Me Me Me n-Pr 1 C₂F₅ —SO₂-(Thien-2-yl) 4-736 Me Me Me Me 2 C₂F₅ —SO₂-(Thien-2-yl) 4-737 Me Me Me Et 2 C₂F₅ —SO₂-(Thien-2-yl) 4-738 Me Me Me n-Pr 2 C₂F₅ —SO₂-(Thien-2-yl) 4-739 Me Me Me Me 0 C₂F₅ —CO—Ph 4-740 Me Me Me Et 0 C₂F₅ —CO—Ph 4-741 Me Me Me n-Pr 0 C₂F₅ —CO—Ph 4-742 Me Me Me Me 1 C₂F₅ —CO—Ph 4-743 Me Me Me Et 1 C₂F₅ —CO—Ph 4-744 Me Me Me n-Pr 1 C₂F₅ —CO—Ph 4-745 Me Me Me Me 2 C₂F₅ —CO—Ph 4-746 Me Me Me Et 2 C₂F₅ —CO—Ph 4-747 Me Me Me n-Pr 2 C₂F₅ —CO—Ph 4-748 Me Me Me Me 0 C₂F₅ —CH₂—CO—Ph 4-749 Me Me Me Et 0 C₂F₅ —CH₂—CO—Ph 4-750 Me Me Me n-Pr 0 C₂F₅ —CH₂—CO—Ph 4-751 Me Me Me Me 1 C₂F₅ —CH₂—CO—Ph 4-752 Me Me Me Et 1 C₂F₅ —CH₂—CO—Ph 4-753 Me Me Me n-Pr 1 C₂F₅ —CH₂—CO—Ph 4-754 Me Me Me Me 2 C₂F₅ —CH₂—CO—Ph 4-755 Me Me Me Et 2 C₂F₅ —CH₂—CO—Ph 4-756 Me Me Me n-Pr 2 C₂F₅ —CH₂—CO—Ph 4-757 Me H Me Me 0 CF(CF₃)₂ —SO₂—n-Pr 4-758 Me H Me Et 0 CF(CF₃)₂ —SO₂—n-Pr 4-759 Me H Me n-Pr 0 CF(CF₃)₂ —SO₂—n-Pr 4-760 Me H Me Me 1 CF(CF₃)₂ —SO₂—n-Pr 4-761 Me H Me Et 1 CF(CF₃)₂ —SO₂—n-Pr 4-762 Me H Me n-Pr 1 CF(CF₃)₂ —SO₂—n-Pr 4-763 Me H Me Me 2 CF(CF₃)₂ —SO₂—n-Pr 4-764 Me H Me Et 2 CF(CF₃)₂ —SO₂—n-Pr 4-765 Me H Me n-Pr 2 CF(CF₃)₂ —SO₂—n-Pr 4-766 Me H Me Me 0 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-767 Me H Me Et 0 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-768 Me H Me n-Pr 0 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-769 Me H Me Me 1 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-770 Me H Me Et 1 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-771 Me H Me n-Pr 1 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-772 Me H Me Me 2 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-773 Me H Me Et 2 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-774 Me H Me n-Pr 2 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-775 Me H Me Me 0 CF(CF₃)₂ —SO₂—Ph 4-776 Me H Me Et 0 CF(CF₃)₂ —SO₂—Ph 4-777 Me H Me n-Pr 0 CF(CF₃)₂ —SO₂—Ph 4-778 Me H Me Me 1 CF(CF₃)₂ —SO₂—Ph 4-779 Me H Me Et 1 CF(CF₃)₂ —SO₂—Ph 4-780 Me H Me n-Pr 1 CF(CF₃)₂ —SO₂—Ph 4-781 Me H Me Me 2 CF(CF₃)₂ —SO₂—Ph 4-782 Me H Me Et 2 CF(CF₃)₂ —SO₂—Ph 4-783 Me H Me n-Pr 2 CF(CF₃)₂ —SO₂—Ph 4-784 Me H Me Me 0 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-785 Me H Me Et 0 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-786 Me H Me n-Pr 0 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-787 Me H Me Me 1 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-788 Me H Me Et 1 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-789 Me H Me n-Pr 1 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-790 Me H Me Me 2 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-791 Me H Me Et 2 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-792 Me H Me n-Pr 2 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-793 Me H Me Me 0 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-794 Me H Me Et 0 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-795 Me H Me n-Pr 0 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-796 Me H Me Me 1 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-797 Me H Me Et 1 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-798 Me H Me n-Pr 1 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-799 Me H Me Me 2 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-800 Me H Me Et 2 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-801 Me H Me n-Pr 2 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-802 Me H Me Me 0 CF(CF₃)₂ —CO—Ph 4-803 Me H Me Et 0 CF(CF₃)₂ —CO—Ph 4-804 Me H Me n-Pr 0 CF(CF₃)₂ —CO—Ph 4-805 Me H Me Me 1 CF(CF₃)₂ —CO—Ph 4-806 Me H Me Et 1 CF(CF₃)₂ —CO—Ph 4-807 Me H Me n-Pr 1 CF(CF₃)₂ —CO—Ph 4-808 Me H Me Me 2 CF(CF₃)₂ —CO—Ph 4-809 Me H Me Et 2 CF(CF₃)₂ —CO—Ph 4-810 Me H Me n-Pr 2 CF(CF₃)₂ —CO—Ph 4-811 Me H Me Me 0 CF(CF₃)₂ —CH₂—CO—Ph 4-812 Me H Me Et 0 CF(CF₃)₂ —CH₂—CO—Ph 4-813 Me H Me n-Pr 0 CF(CF₃)₂ —CH₂—CO—Ph 4-814 Me H Me Me 1 CF(CF₃)₂ —CH₂—CO—Ph 4-815 Me H Me Et 1 CF(CF₃)₂ —CH₂—CO—Ph 4-816 Me H Me n-Pr 1 CF(CF₃)₂ —CH₂—CO—Ph 4-817 Me H Me Me 2 CF(CF₃)₂ —CH₂—CO—Ph 4-818 Me H Me Et 2 CF(CF₃)₂ —CH₂—CO—Ph 4-819 Me H Me n-Pr 2 CF(CF₃)₂ —CH₂—CO—Ph 4-820 Et H Me Me 0 CF(CF₃)₂ —SO₂—n-Pr 4-821 Et H Me Et 0 CF(CF₃)₂ —SO₂—n-Pr 4-822 Et H Me n-Pr 0 CF(CF₃)₂ —SO₂—n-Pr 4-823 Et H Me Me 1 CF(CF₃)₂ —SO₂—n-Pr 4-824 Et H Me Et 1 CF(CF₃)₂ —SO₂—n-Pr 4-825 Et H Me n-Pr 1 CF(CF₃)₂ —SO₂—n-Pr 4-826 Et H Me Me 2 CF(CF₃)₂ —SO₂—n-Pr 4-827 Et H Me Et 2 CF(CF₃)₂ —SO₂—n-Pr 4-828 Et H Me n-Pr 2 CF(CF₃)₂ —SO₂—n-Pr 4-829 Et H Me Me 0 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-830 Et H Me Et 0 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-831 Et H Me n-Pr 0 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-832 Et H Me Me 1 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-833 Et H Me Et 1 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-834 Et H Me n-Pr 1 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-835 Et H Me Me 2 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-836 Et H Me Et 2 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-837 Et H Me n-Pr 2 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-838 Et H Me Me 0 CF(CF₃)₂ —SO₂—Ph 4-839 Et H Me Et 0 CF(CF₃)₂ —SO₂—Ph 4-840 Et H Me n-Pr 0 CF(CF₃)₂ —SO₂—Ph 4-841 Et H Me Me 1 CF(CF₃)₂ —SO₂—Ph 4-842 Et H Me Et 1 CF(CF₃)₂ —SO₂—Ph 4-843 Et H Me n-Pr 1 CF(CF₃)₂ —SO₂—Ph 4-844 Et H Me Me 2 CF(CF₃)₂ —SO₂—Ph 4-845 Et H Me Et 2 CF(CF₃)₂ —SO₂—Ph 4-846 Et H Me n-Pr 2 CF(CF₃)₂ —SO₂—Ph 4-847 Et H Me Me 0 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-848 Et H Me Et 0 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-849 Et H Me n-Pr 0 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-850 Et H Me Me 1 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-851 Et H Me Et 1 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-852 Et H Me n-Pr 1 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-853 Et H Me Me 2 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-854 Et H Me Et 2 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-855 Et H Me n-Pr 2 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-856 Et H Me Me 0 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-857 Et H Me Et 0 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-858 Et H Me n-Pr 0 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-859 Et H Me Me 1 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-860 Et H Me Et 1 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-861 Et H Me n-Pr 1 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-862 Et H Me Me 2 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-863 Et H Me Et 2 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-864 Et H Me n-Pr 2 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-865 Et H Me Me 0 CF(CF₃)₂ —CO—Ph 4-866 Et H Me Et 0 CF(CF₃)₂ —CO—Ph 4-867 Et H Me n-Pr 0 CF(CF₃)₂ —CO—Ph 4-868 Et H Me Me 1 CF(CF₃)₂ —CO—Ph 4-869 Et H Me Et 1 CF(CF₃)₂ —CO—Ph 4-870 Et H Me n-Pr 1 CF(CF₃)₂ —CO—Ph 4-871 Et H Me Me 2 CF(CF₃)₂ —CO—Ph 4-872 Et H Me Et 2 CF(CF₃)₂ —CO—Ph 4-873 Et H Me n-Pr 2 CF(CF₃)₂ —CO—Ph 4-874 Et H Me Me 0 CF(CF₃)₂ —CH₂—CO—Ph 4-875 Et H Me Et 0 CF(CF₃)₂ —CH₂—CO—Ph 4-876 Et H Me n-Pr 0 CF(CF₃)₂ —CH₂—CO—Ph 4-877 Et H Me Me 1 CF(CF₃)₂ —CH₂—CO—Ph 4-878 Et H Me Et 1 CF(CF₃)₂ —CH₂—CO—Ph 4-879 Et H Me n-Pr 1 CF(CF₃)₂ —CH₂—CO—Ph 4-880 Et H Me Me 2 CF(CF₃)₂ —CH₂—CO—Ph 4-881 Et H Me Et 2 CF(CF₃)₂ —CH₂—CO—Ph 4-882 Et H Me n-Pr 2 CF(CF₃)₂ —CH₂—CO—Ph 4-883 Me Me Me Me 0 CF(CF₃)₂ —SO₂—n-Pr 4-884 Me Me Me Et 0 CF(CF₃)₂ —SO₂—n-Pr 4-885 Me Me Me n-Pr 0 CF(CF₃)₂ —SO₂—n-Pr 4-886 Me Me Me Me 1 CF(CF₃)₂ —SO₂—n-Pr 4-887 Me Me Me Et 1 CF(CF₃)₂ —SO₂—n-Pr 4-888 Me Me Me n-Pr 1 CF(CF₃)₂ —SO₂—n-Pr 4-889 Me Me Me Me 2 CF(CF₃)₂ —SO₂—n-Pr 4-890 Me Me Me Et 2 CF(CF₃)₂ —SO₂—n-Pr 4-891 Me Me Me n-Pr 2 CF(CF₃)₂ —SO₂—n-Pr 4-892 Me Me Me Me 0 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-893 Me Me Me Et 0 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-894 Me Me Me n-Pr 0 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-895 Me Me Me Me 1 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-896 Me Me Me Et 1 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-897 Me Me Me n-Pr 1 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-898 Me Me Me Me 2 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-899 Me Me Me Et 2 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-900 Me Me Me n-Pr 2 CF(CF₃)₂ —SO₂—(CH₂)₂OMe 4-901 Me Me Me Me 0 CF(CF₃)₂ —SO₂—Ph 4-902 Me Me Me Et 0 CF(CF₃)₂ —SO₂—Ph 4-903 Me Me Me n-Pr 0 CF(CF₃)₂ —SO₂—Ph 4-904 Me Me Me Me 1 CF(CF₃)₂ —SO₂—Ph 4-905 Me Me Me Et 1 CF(CF₃)₂ —SO₂—Ph 4-906 Me Me Me n-Pr 1 CF(CF₃)₂ —SO₂—Ph 4-907 Me Me Me Me 2 CF(CF₃)₂ —SO₂—Ph 4-908 Me Me Me Et 2 CF(CF₃)₂ —SO₂—Ph 4-909 Me Me Me n-Pr 2 CF(CF₃)₂ —SO₂—Ph 4-910 Me Me Me Me 0 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-911 Me Me Me Et 0 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-912 Me Me Me n-Pr 0 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-913 Me Me Me Me 1 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-914 Me Me Me Et 1 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-915 Me Me Me n-Pr 1 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-916 Me Me Me Me 2 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-917 Me Me Me Et 2 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-918 Me Me Me n-Pr 2 CF(CF₃)₂ —SO₂—(4-Me—Ph) 4-919 Me Me Me Me 0 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-920 Me Me Me Et 0 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-921 Me Me Me n-Pr 0 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-922 Me Me Me Me 1 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-923 Me Me Me Et 1 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-924 Me Me Me n-Pr 1 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-925 Me Me Me Me 2 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-926 Me Me Me Et 2 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-927 Me Me Me n-Pr 2 CF(CF₃)₂ —SO₂-(Thien-2-yl) 4-928 Me Me Me Me 0 CF(CF₃)₂ —CO—Ph 4-929 Me Me Me Et 0 CF(CF₃)₂ —CO—Ph 4-930 Me Me Me n-Pr 0 CF(CF₃)₂ —CO—Ph 4-931 Me Me Me Me 1 CF(CF₃)₂ —CO—Ph 4-932 Me Me Me Et 1 CF(CF₃)₂ —CO—Ph 4-933 Me Me Me n-Pr 1 CF(CF₃)₂ —CO—Ph 4-934 Me Me Me Me 2 CF(CF₃)₂ —CO—Ph 4-935 Me Me Me Et 2 CF(CF₃)₂ —CO—Ph 4-936 Me Me Me n-Pr 2 CF(CF₃)₂ —CO—Ph 4-937 Me Me Me Me 0 CF(CF₃)₂ —CH₂—CO—Ph 4-938 Me Me Me Et 0 CF(CF₃)₂ —CH₂—CO—Ph 4-939 Me Me Me n-Pr 0 CF(CF₃)₂ —CH₂—CO—Ph 4-940 Me Me Me Me 1 CF(CF₃)₂ —CH₂—CO—Ph 4-941 Me Me Me Et 1 CF(CF₃)₂ —CH₂—CO—Ph 4-942 Me Me Me n-Pr 1 CF(CF₃)₂ —CH₂—CO—Ph 4-943 Me Me Me Me 2 CF(CF₃)₂ —CH₂—CO—Ph 4-944 Me Me Me Et 2 CF(CF₃)₂ —CH₂—CO—Ph 4-945 Me Me Me n-Pr 2 CF(CF₃)₂ —CH₂—CO—Ph 4-946 Me H Me Me 0 CHF₂ —SO₂—n-Pr 4-947 Me H Me Et 0 CHF₂ —SO₂—n-Pr 4-948 Me H Me n-Pr 0 CHF₂ —SO₂—n-Pr 4-949 Me H Me Me 1 CHF₂ —SO₂—n-Pr 4-950 Me H Me Et 1 CHF₂ —SO₂—n-Pr 4-951 Me H Me n-Pr 1 CHF₂ —SO₂—n-Pr 4-952 Me H Me Me 2 CHF₂ —SO₂—n-Pr 4-953 Me H Me Et 2 CHF₂ —SO₂—n-Pr 4-954 Me H Me n-Pr 2 CHF₂ —SO₂—n-Pr 4-955 Me H Me Me 0 CHF₂ —SO₂—(CH₂)₂OMe 4-956 Me H Me Et 0 CHF₂ —SO₂—(CH₂)₂OMe 4-957 Me H Me n-Pr 0 CHF₂ —SO₂—(CH₂)₂OMe 4-958 Me H Me Me 1 CHF₂ —SO₂—(CH₂)₂OMe 4-959 Me H Me Et 1 CHF₂ —SO₂—(CH₂)₂OMe 4-960 Me H Me n-Pr 1 CHF₂ —SO₂—(CH₂)₂OMe 4-961 Me H Me Me 2 CHF₂ —SO₂—(CH₂)₂OMe 4-962 Me H Me Et 2 CHF₂ —SO₂—(CH₂)₂OMe 4-963 Me H Me n-Pr 2 CHF₂ —SO₂—(CH₂)₂OMe 4-964 Me H Me Me 0 CHF₂ —SO₂—Ph 4-965 Me H Me Et 0 CHF₂ —SO₂—Ph 4-966 Me H Me n-Pr 0 CHF₂ —SO₂—Ph 4-967 Me H Me Me 1 CHF₂ —SO₂—Ph 4-968 Me H Me Et 1 CHF₂ —SO₂—Ph 4-969 Me H Me n-Pr 1 CHF₂ —SO₂—Ph 4-970 Me H Me Me 2 CHF₂ —SO₂—Ph 4-971 Me H Me Et 2 CHF₂ —SO₂—Ph 4-972 Me H Me n-Pr 2 CHF₂ —SO₂—Ph 4-973 Me H Me Me 0 CHF₂ —SO₂—(4-Me—Ph) 4-974 Me H Me Et 0 CHF₂ —SO₂—(4-Me—Ph) 4-975 Me H Me n-Pr 0 CHF₂ —SO₂—(4-Me—Ph) 4-976 Me H Me Me 1 CHF₂ —SO₂—(4-Me—Ph) 4-977 Me H Me Et 1 CHF₂ —SO₂—(4-Me—Ph) 4-978 Me H Me n-Pr 1 CHF₂ —SO₂—(4-Me—Ph) 4-979 Me H Me Me 2 CHF₂ —SO₂—(4-Me—Ph) 4-980 Me H Me Et 2 CHF₂ —SO₂—(4-Me—Ph) 4-981 Me H Me n-Pr 2 CHF₂ —SO₂—(4-Me—Ph) 4-982 Me H Me Me 0 CHF₂ —SO₂-(Thien-2-yl) 4-983 Me H Me Et 0 CHF₂ —SO₂-(Thien-2-yl) 4-984 Me H Me n-Pr 0 CHF₂ —SO₂-(Thien-2-yl) 4-985 Me H Me Me 1 CHF₂ —SO₂-(Thien-2-yl) 4-986 Me H Me Et 1 CHF₂ —SO₂-(Thien-2-yl) 4-987 Me H Me n-Pr 1 CHF₂ —SO₂-(Thien-2-yl) 4-988 Me H Me Me 2 CHF₂ —SO₂-(Thien-2-yl) 4-989 Me H Me Et 2 CHF₂ —SO₂-(Thien-2-yl) 4-990 Me H Me n-Pr 2 CHF₂ —SO₂-(Thien-2-yl) 4-991 Me H Me Me 0 CHF₂ —CO—Ph 4-992 Me H Me Et 0 CHF₂ —CO—Ph 4-993 Me H Me n-Pr 0 CHF₂ —CO—Ph 4-994 Me H Me Me 1 CHF₂ —CO—Ph 4-995 Me H Me Et 1 CHF₂ —CO—Ph 4-996 Me H Me n-Pr 1 CHF₂ —CO—Ph 4-997 Me H Me Me 2 CHF₂ —CO—Ph 4-998 Me H Me Et 2 CHF₂ —CO—Ph 4-999 Me H Me n-Pr 2 CHF₂ —CO—Ph 4-1000 Me H Me Me 0 CHF₂ —CH₂—CO—Ph 4-1001 Me H Me Et 0 CHF₂ —CH₂—CO—Ph 4-1002 Me H Me n-Pr 0 CHF₂ —CH₂—CO—Ph 4-1003 Me H Me Me 1 CHF₂ —CH₂—CO—Ph 4-1004 Me H Me Et 1 CHF₂ —CH₂—CO—Ph 4-1005 Me H Me n-Pr 1 CHF₂ —CH₂—CO—Ph 4-1006 Me H Me Me 2 CHF₂ —CH₂—CO—Ph 4-1007 Me H Me Et 2 CHF₂ —CH₂—CO—Ph 4-1008 Me H Me n-Pr 2 CHF₂ —CH₂—CO—Ph 4-1009 Et H Me Me 0 CHF₂ —SO₂—n-Pr 4-1010 Et H Me Et 0 CHF₂ —SO₂—n-Pr 4-1011 Et H Me n-Pr 0 CHF₂ —SO₂—n-Pr 4-1012 Et H Me Me 1 CHF₂ —SO₂—n-Pr 4-1013 Et H Me Et 1 CHF₂ —SO₂—n-Pr 4-1014 Et H Me n-Pr 1 CHF₂ —SO₂—n-Pr 4-1015 Et H Me Me 2 CHF₂ —SO₂—n-Pr 4-1016 Et H Me Et 2 CHF₂ —SO₂—n-Pr 4-1017 Et H Me n-Pr 2 CHF₂ —SO₂—n-Pr 4-1018 Et H Me Me 0 CHF₂ —SO₂—(CH₂)₂OMe 4-1019 Et H Me Et 0 CHF₂ —SO₂—(CH₂)₂OMe 4-1020 Et H Me n-Pr 0 CHF₂ —SO₂—(CH₂)₂OMe 4-1021 Et H Me Me 1 CHF₂ —SO₂—(CH₂)₂OMe 4-1022 Et H Me Et 1 CHF₂ —SO₂—(CH₂)₂OMe 4-1023 Et H Me n-Pr 1 CHF₂ —SO₂—(CH₂)₂OMe 4-1024 Et H Me Me 2 CHF₂ —SO₂—(CH₂)₂OMe 4-1025 Et H Me Et 2 CHF₂ —SO₂—(CH₂)₂OMe 4-1026 Et H Me n-Pr 2 CHF₂ —SO₂—(CH₂)₂OMe 4-1027 Et H Me Me 0 CHF₂ —SO₂—Ph 4-1028 Et H Me Et 0 CHF₂ —SO₂—Ph 4-1029 Et H Me n-Pr 0 CHF₂ —SO₂—Ph 4-1030 Et H Me Me 1 CHF₂ —SO₂—Ph 4-1031 Et H Me Et 1 CHF₂ —SO₂—Ph 4-1032 Et H Me n-Pr 1 CHF₂ —SO₂—Ph 4-1033 Et H Me Me 2 CHF₂ —SO₂—Ph 4-1034 Et H Me Et 2 CHF₂ —SO₂—Ph 4-1035 Et H Me n-Pr 2 CHF₂ —SO₂—Ph 4-1036 Et H Me Me 0 CHF₂ —SO₂—(4-Me—Ph) 4-1037 Et H Me Et 0 CHF₂ —SO₂—(4-Me—Ph) 4-1038 Et H Me n-Pr 0 CHF₂ —SO₂—(4-Me—Ph) 4-1039 Et H Me Me 1 CHF₂ —SO₂—(4-Me—Ph) 4-1040 Et H Me Et 1 CHF₂ —SO₂—(4-Me—Ph) 4-1041 Et H Me n-Pr 1 CHF₂ —SO₂—(4-Me—Ph) 4-1042 Et H Me Me 2 CHF₂ —SO₂—(4-Me—Ph) 4-1043 Et H Me Et 2 CHF₂ —SO₂—(4-Me—Ph) 4-1044 Et H Me n-Pr 2 CHF₂ —SO₂—(4-Me—Ph) 4-1045 Et H Me Me 0 CHF₂ —SO₂-(Thien-2-yl) 4-1046 Et H Me Et 0 CHF₂ —SO₂-(Thien-2-yl) 4-1047 Et H Me n-Pr 0 CHF₂ —SO₂-(Thien-2-yl) 4-1048 Et H Me Me 1 CHF₂ —SO₂-(Thien-2-yl) 4-1049 Et H Me Et 1 CHF₂ —SO₂-(Thien-2-yl) 4-1050 Et H Me n-Pr 1 CHF₂ —SO₂-(Thien-2-yl) 4-1051 Et H Me Me 2 CHF₂ —SO₂-(Thien-2-yl) 4-1052 Et H Me Et 2 CHF₂ —SO₂-(Thien-2-yl) 4-1053 Et H Me n-Pr 2 CHF₂ —SO₂-(Thien-2-yl) 4-1054 Et H Me Me 0 CHF₂ —CO—Ph 4-1055 Et H Me Et 0 CHF₂ —CO—Ph 4-1056 Et H Me n-Pr 0 CHF₂ —CO—Ph 4-1057 Et H Me Me 1 CHF₂ —CO—Ph 4-1058 Et H Me Et 1 CHF₂ —CO—Ph 4-1059 Et H Me n-Pr 1 CHF₂ —CO—Ph 4-1060 Et H Me Me 2 CHF₂ —CO—Ph 4-1061 Et H Me Et 2 CHF₂ —CO—Ph 4-1062 Et H Me n-Pr 2 CHF₂ —CO—Ph 4-1063 Et H Me Me 0 CHF₂ —CH₂—CO—Ph 4-1064 Et H Me Et 0 CHF₂ —CH₂—CO—Ph 4-1065 Et H Me n-Pr 0 CHF₂ —CH₂—CO—Ph 4-1066 Et H Me Me 1 CHF₂ —CH₂—CO—Ph 4-1067 Et H Me Et 1 CHF₂ —CH₂—CO—Ph 4-1068 Et H Me n-Pr 1 CHF₂ —CH₂—CO—Ph 4-1069 Et H Me Me 2 CHF₂ —CH₂—CO—Ph 4-1070 Et H Me Et 2 CHF₂ —CH₂—CO—Ph 4-1071 Et H Me n-Pr 2 CHF₂ —CH₂—CO—Ph 4-1072 Me Me Me Me 0 CHF₂ —SO₂—n-Pr 4-1073 Me Me Me Et 0 CHF₂ —SO₂—n-Pr 4-1074 Me Me Me n-Pr 0 CHF₂ —SO₂—n-Pr 4-1075 Me Me Me Me 1 CHF₂ —SO₂—n-Pr 4-1076 Me Me Me Et 1 CHF₂ —SO₂—n-Pr 4-1077 Me Me Me n-Pr 1 CHF₂ —SO₂—n-Pr 4-1078 Me Me Me Me 2 CHF₂ —SO₂—n-Pr 4-1079 Me Me Me Et 2 CHF₂ —SO₂—n-Pr 4-1080 Me Me Me n-Pr 2 CHF₂ —SO₂—n-Pr 4-1081 Me Me Me Me 0 CHF₂ —SO₂—(CH₂)₂OMe 4-1082 Me Me Me Et 0 CHF₂ —SO₂—(CH₂)₂OMe 4-1083 Me Me Me n-Pr 0 CHF₂ —SO₂—(CH₂)₂OMe 4-1084 Me Me Me Me 1 CHF₂ —SO₂—(CH₂)₂OMe 4-1085 Me Me Me Et 1 CHF₂ —SO₂—(CH₂)₂OMe 4-1086 Me Me Me n-Pr 1 CHF₂ —SO₂—(CH₂)₂OMe 4-1087 Me Me Me Me 2 CHF₂ —SO₂—(CH₂)₂OMe 4-1088 Me Me Me Et 2 CHF₂ —SO₂—(CH₂)₂OMe 4-1089 Me Me Me n-Pr 2 CHF₂ —SO₂—(CH₂)₂OMe 4-1090 Me Me Me Me 0 CHF₂ —SO₂—Ph 4-1091 Me Me Me Et 0 CHF₂ —SO₂—Ph 4-1092 Me Me Me n-Pr 0 CHF₂ —SO₂—Ph 4-1093 Me Me Me Me 1 CHF₂ —SO₂—Ph 4-1094 Me Me Me Et 1 CHF₂ —SO₂—Ph 4-1095 Me Me Me n-Pr 1 CHF₂ —SO₂—Ph 4-1096 Me Me Me Me 2 CHF₂ —SO₂—Ph 4-1097 Me Me Me Et 2 CHF₂ —SO₂—Ph 4-1098 Me Me Me n-Pr 2 CHF₂ —SO₂—Ph 4-1099 Me Me Me Me 0 CHF₂ —SO₂—(4-Me—Ph) 4-1100 Me Me Me Et 0 CHF₂ —SO₂—(4-Me—Ph) 4-1101 Me Me Me n-Pr 0 CHF₂ —SO₂—(4-Me—Ph) 4-1102 Me Me Me Me 1 CHF₂ —SO₂—(4-Me—Ph) 4-1103 Me Me Me Et 1 CHF₂ —SO₂—(4-Me—Ph) 4-1104 Me Me Me n-Pr 1 CHF₂ —SO₂—(4-Me—Ph) 4-1105 Me Me Me Me 2 CHF₂ —SO₂—(4-Me—Ph) 4-1106 Me Me Me Et 2 CHF₂ —SO₂—(4-Me—Ph) 4-1107 Me Me Me n-Pr 2 CHF₂ —SO₂—(4-Me—Ph) 4-1108 Me Me Me Me 0 CHF₂ —SO₂-(Thien-2-yl) 4-1109 Me Me Me Et 0 CHF₂ —SO₂-(Thien-2-yl) 4-1110 Me Me Me n-Pr 0 CHF₂ —SO₂-(Thien-2-yl) 4-1111 Me Me Me Me 1 CHF₂ —SO₂-(Thien-2-yl) 4-1112 Me Me Me Et 1 CHF₂ —SO₂-(Thien-2-yl) 4-1113 Me Me Me n-Pr 1 CHF₂ —SO₂-(Thien-2-yl) 4-1114 Me Me Me Me 2 CHF₂ —SO₂-(Thien-2-yl) 4-1115 Me Me Me Et 2 CHF₂ —SO₂-(Thien-2-yl) 4-1116 Me Me Me n-Pr 2 CHF₂ —SO₂-(Thien-2-yl) 4-1117 Me Me Me Me 0 CHF₂ —CO—Ph 4-1118 Me Me Me Et 0 CHF₂ —CO—Ph 4-1119 Me Me Me n-Pr 0 CHF₂ —CO—Ph 4-1120 Me Me Me Me 1 CHF₂ —CO—Ph 4-1121 Me Me Me Et 1 CHF₂ —CO—Ph 4-1122 Me Me Me n-Pr 1 CHF₂ —CO—Ph 4-1123 Me Me Me Me 2 CHF₂ —CO—Ph 4-1124 Me Me Me Et 2 CHF₂ —CO—Ph 4-1125 Me Me Me n-Pr 2 CHF₂ —CO—Ph 4-1126 Me Me Me Me 0 CHF₂ —CH₂—CO—Ph 4-1127 Me Me Me Et 0 CHF₂ —CH₂—CO—Ph 4-1128 Me Me Me n-Pr 0 CHF₂ —CH₂—CO—Ph 4-1129 Me Me Me Me 1 CHF₂ —CH₂—CO—Ph 4-1130 Me Me Me Et 1 CHF₂ —CH₂—CO—Ph 4-1131 Me Me Me n-Pr 1 CHF₂ —CH₂—CO—Ph 4-1132 Me Me Me Me 2 CHF₂ —CH₂—CO—Ph 4-1133 Me Me Me Et 2 CHF₂ —CH₂—CO—Ph 4-1134 Me Me Me n-Pr 2 CHF₂ —CH₂—CO—Ph

TABLE 5 Inventive compounds of the formula (IIIa),

No. X R¹ n Y Physical data: ¹H-NMR: δ [DMSO-d₆] 5-1 Me Me 0 CF₂Cl 5-2 Me Et 0 CF₂Cl 5-3 Me n-Pr 0 CF₂Cl 5-4 Me i-Pr 0 CF₂Cl 5-5 Me n-Bu 0 CF₂Cl 5-6 Me i-Bu 0 CF₂Cl 5-7 Me s-Bu 0 CF₂Cl 5-8 Me t-Bu 0 CF₂Cl 5-9 Me Me 1 CF₂Cl 5-10 Me Et 1 CF₂Cl 5-11 Me n-Pr 1 CF₂Cl 5-12 Me i-Pr 1 CF₂Cl 5-13 Me n-Bu 1 CF₂Cl 5-14 Me i-Bu 1 CF₂Cl 5-15 Me s-Bu 1 CF₂Cl 5-16 Me t-Bu 1 CF₂Cl 5-17 Me Me 2 CF₂Cl 5-18 Me Et 2 CF₂Cl 5-19 Me n-Pr 2 CF₂Cl 5-20 Me i-Pr 2 CF₂Cl 5-21 Me n-Bu 2 CF₂Cl 5-22 Me i-Bu 2 CF₂Cl 5-23 Me s-Bu 2 CF₂Cl 5-24 Me t-Bu 2 CF₂Cl 5-25 Et Me 0 CF₂Cl 5-26 Et Et 0 CF₂Cl 5-27 Et n-Pr 0 CF₂Cl 5-28 Et i-Pr 0 CF₂Cl 5-29 Et n-Bu 0 CF₂Cl 5-30 Et i-Bu 0 CF₂Cl 5-31 Et s-Bu 0 CF₂Cl 5-32 Et t-Bu 0 CF₂Cl 5-33 Et Me 1 CF₂Cl 5-34 Et Et 1 CF₂Cl 5-35 Et n-Pr 1 CF₂Cl 5-36 Et i-Pr 1 CF₂Cl 5-37 Et n-Bu 1 CF₂Cl 5-38 Et i-Bu 1 CF₂Cl 5-39 Et s-Bu 1 CF₂Cl 5-40 Et t-Bu 1 CF₂Cl 5-41 Et Me 2 CF₂Cl 5-42 Et Et 2 CF₂Cl 5-43 Et n-Pr 2 CF₂Cl 5-44 Et i-Pr 2 CF₂Cl 5-45 Et n-Bu 2 CF₂Cl 5-46 Et i-Bu 2 CF₂Cl 5-47 Et s-Bu 2 CF₂Cl 5-48 Et t-Bu 2 CF₂Cl 5-49 Me Me 0 CFCl₂ 5-50 Me Et 0 CFCl₂ 5-51 Me n-Pr 0 CFCl₂ 5-52 Me i-Pr 0 CFCl₂ 5-53 Me n-Bu 0 CFCl₂ 5-54 Me i-Bu 0 CFCl₂ 5-55 Me s-Bu 0 CFCl₂ 5-56 Me t-Bu 0 CFCl₂ 5-57 Me Me 1 CFCl₂ 5-58 Me Et 1 CFCl₂ 5-59 Me n-Pr 1 CFCl₂ 5-60 Me i-Pr 1 CFCl₂ 5-61 Me n-Bu 1 CFCl₂ 5-62 Me i-Bu 1 CFCl₂ 5-63 Me s-Bu 1 CFCl₂ 5-64 Me t-Bu 1 CFCl₂ 5-65 Me Me 2 CFCl₂ 5-66 Me Et 2 CFCl₂ 5-67 Me n-Pr 2 CFCl₂ 5-68 Me i-Pr 2 CFCl₂ 5-69 Me n-Bu 2 CFCl₂ 5-70 Me i-Bu 2 CFCl₂ 5-71 Me s-Bu 2 CFCl₂ 5-72 Me t-Bu 2 CFCl₂ 5-73 Et Me 0 CFCl₂ 5-74 Et Et 0 CFCl₂ 5-75 Et n-Pr 0 CFCl₂ 5-76 Et i-Pr 0 CFCl₂ 5-77 Et n-Bu 0 CFCl₂ 5-78 Et i-Bu 0 CFCl₂ 5-79 Et s-Bu 0 CFCl₂ 5-80 Et t-Bu 0 CFCl₂ 5-81 Et Me 1 CFCl₂ 5-82 Et Et 1 CFCl₂ 5-83 Et n-Pr 1 CFCl₂ 5-84 Et i-Pr 1 CFCl₂ 5-85 Et n-Bu 1 CFCl₂ 5-86 Et i-Bu 1 CFCl₂ 5-87 Et s-Bu 1 CFCl₂ 5-88 Et t-Bu 1 CFCl₂ 5-89 Et Me 2 CFCl₂ 5-90 Et Et 2 CFCl₂ 5-91 Et n-Pr 2 CFCl₂ 5-92 Et i-Pr 2 CFCl₂ 5-93 Et n-Bu 2 CFCl₂ 5-94 Et i-Bu 2 CFCl₂ 5-95 Et s-Bu 2 CFCl₂ 5-96 Et t-Bu 2 CFCl₂ 5-97 Me Me 0 CCl₃ 5-98 Me Et 0 CCl₃ 5-99 Me n-Pr 0 CCl₃ 5-100 Me i-Pr 0 CCl₃ 5-101 Me n-Bu 0 CCl₃ 5-102 Me i-Bu 0 CCl₃ 5-103 Me s-Bu 0 CCl₃ 5-104 Me t-Bu 0 CCl₃ 5-105 Me Me 1 CCl₃ 5-106 Me Et 1 CCl₃ 5-107 Me n-Pr 1 CCl₃ 5-108 Me i-Pr 1 CCl₃ 5-109 Me n-Bu 1 CCl₃ 5-110 Me i-Bu 1 CCl₃ 5-111 Me s-Bu 1 CCl₃ 5-112 Me t-Bu 1 CCl₃ 5-113 Me Me 2 CCl₃ 5-114 Me Et 2 CCl₃ 5-115 Me n-Pr 2 CCl₃ 5-116 Me i-Pr 2 CCl₃ 5-117 Me n-Bu 2 CCl₃ 5-118 Me i-Bu 2 CCl₃ 5-119 Me s-Bu 2 CCl₃ 5-120 Me t-Bu 2 CCl₃ 5-121 Et Me 0 CCl₃ 5-122 Et Et 0 CCl₃ 5-123 Et n-Pr 0 CCl₃ 5-124 Et i-Pr 0 CCl₃ 5-125 Et n-Bu 0 CCl₃ 5-126 Et i-Bu 0 CCl₃ 5-127 Et s-Bu 0 CCl₃ 5-128 Et t-Bu 0 CCl₃ 5-129 Et Me 1 CCl₃ 5-130 Et Et 1 CCl₃ 5-131 Et n-Pr 1 CCl₃ 5-132 Et i-Pr 1 CCl₃ 5-133 Et n-Bu 1 CCl₃ 5-134 Et i-Bu 1 CCl₃ 5-135 Et s-Bu 1 CCl₃ 5-136 Et t-Bu 1 CCl₃ 5-137 Et Me 2 CCl₃ 5-138 Et Et 2 CCl₃ 5-139 Et n-Pr 2 CCl₃ 5-140 Et i-Pr 2 CCl₃ 5-141 Et n-Bu 2 CCl₃ 5-142 Et i-Bu 2 CCl₃ 5-143 Et s-Bu 2 CCl₃ 5-144 Et t-Bu 2 CCl₃ 5-145 Me Me 0 C₂F₅ 7.84 (d, 1H), 7.65 (d, 1H), 2.76 (s, 3H), 2.27 (s, 3H) 5-146 Me Et 0 C₂F₅ 5-147 Me n-Pr 0 C₂F₅ 5-148 Me i-Pr 0 C₂F₅ 5-149 Me n-Bu 0 C₂F₅ 5-150 Me i-Bu 0 C₂F₅ 5-151 Me s-Bu 0 C₂F₅ 5-152 Me t-Bu 0 C₂F₅ 5-153 Me Me 1 C₂F₅ 5-154 Me Et 1 C₂F₅ 5-155 Me n-Pr 1 C₂F₅ 5-156 Me i-Pr 1 C₂F₅ 5-157 Me n-Bu 1 C₂F₅ 5-158 Me i-Bu 1 C₂F₅ 5-159 Me s-Bu 1 C₂F₅ 5-160 Me t-Bu 1 C₂F₅ 5-161 Me Me 2 C₂F₅ 8.03 (d, 1H), 7.82 (d, 1H), 3.44 (s, 3H), 2.74 (s, 3H) 5-162 Me Et 2 C₂F₅ 5-163 Me n-Pr 2 C₂F₅ 5-164 Me i-Pr 2 C₂F₅ 5-165 Me n-Bu 2 C₂F₅ 5-166 Me i-Bu 2 C₂F₅ 5-167 Me s-Bu 2 C₂F₅ 5-168 Me t-Bu 2 C₂F₅ 5-169 Et Me 0 C₂F₅ 5-170 Et Et 0 C₂F₅ 5-171 Et n-Pr 0 C₂F₅ 5-172 Et i-Pr 0 C₂F₅ 5-173 Et n-Bu 0 C₂F₅ 5-174 Et i-Bu 0 C₂F₅ 5-175 Et s-Bu 0 C₂F₅ 5-176 Et t-Bu 0 C₂F₅ 5-177 Et Me 1 C₂F₅ 5-178 Et Et 1 C₂F₅ 5-179 Et n-Pr 1 C₂F₅ 5-180 Et i-Pr 1 C₂F₅ 5-181 Et n-Bu 1 C₂F₅ 5-182 Et i-Bu 1 C₂F₅ 5-183 Et s-Bu 1 C₂F₅ 5-184 Et t-Bu 1 C₂F₅ 5-185 Et Me 2 C₂F₅ 5-186 Et Et 2 C₂F₅ 5-187 Et n-Pr 2 C₂F₅ 5-188 Et i-Pr 2 C₂F₅ 5-189 Et n-Bu 2 C₂F₅ 5-190 Et i-Bu 2 C₂F₅ 5-191 Et s-Bu 2 C₂F₅ 5-192 Et t-Bu 2 C₂F₅ 5-193 Me Me 0 CF(CF₃)₂ 5-194 Me Et 0 CF(CF₃)₂ 5-195 Me n-Pr 0 CF(CF₃)₂ 5-196 Me i-Pr 0 CF(CF₃)₂ 5-197 Me n-Bu 0 CF(CF₃)₂ 5-198 Me i-Bu 0 CF(CF₃)₂ 5-199 Me s-Bu 0 CF(CF₃)₂ 5-200 Me t-Bu 0 CF(CF₃)₂ 5-201 Me Me 1 CF(CF₃)₂ 5-202 Me Et 1 CF(CF₃)₂ 5-203 Me n-Pr 1 CF(CF₃)₂ 5-204 Me i-Pr 1 CF(CF₃)₂ 5-205 Me n-Bu 1 CF(CF₃)₂ 5-206 Me i-Bu 1 CF(CF₃)₂ 5-207 Me s-Bu 1 CF(CF₃)₂ 5-208 Me t-Bu 1 CF(CF₃)₂ 5-209 Me Me 2 CF(CF₃)₂ 5-210 Me Et 2 CF(CF₃)₂ 5-211 Me n-Pr 2 CF(CF₃)₂ 5-212 Me i-Pr 2 CF(CF₃)₂ 5-213 Me n-Bu 2 CF(CF₃)₂ 5-214 Me i-Bu 2 CF(CF₃)₂ 5-215 Me s-Bu 2 CF(CF₃)₂ 5-216 Me t-Bu 2 CF(CF₃)₂ 5-217 Et Me 0 CF(CF₃)₂ 5-218 Et Et 0 CF(CF₃)₂ 5-219 Et n-Pr 0 CF(CF₃)₂ 5-220 Et i-Pr 0 CF(CF₃)₂ 5-221 Et n-Bu 0 CF(CF₃)₂ 5-222 Et i-Bu 0 CF(CF₃)₂ 5-223 Et s-Bu 0 CF(CF₃)₂ 5-224 Et t-Bu 0 CF(CF₃)₂ 5-225 Et Me 1 CF(CF₃)₂ 5-226 Et Et 1 CF(CF₃)₂ 5-227 Et n-Pr 1 CF(CF₃)₂ 5-228 Et i-Pr 1 CF(CF₃)₂ 5-229 Et n-Bu 1 CF(CF₃)₂ 5-230 Et i-Bu 1 CF(CF₃)₂ 5-231 Et s-Bu 1 CF(CF₃)₂ 5-232 Et t-Bu 1 CF(CF₃)₂ 5-233 Et Me 2 CF(CF₃)₂ 5-234 Et Et 2 CF(CF₃)₂ 5-235 Et n-Pr 2 CF(CF₃)₂ 5-236 Et i-Pr 2 CF(CF₃)₂ 5-237 Et n-Bu 2 CF(CF₃)₂ 5-238 Et i-Bu 2 CF(CF₃)₂ 5-239 Et s-Bu 2 CF(CF₃)₂ 5-240 Et t-Bu 2 CF(CF₃)₂ 5-241 Me Me 0 CHF₂ 5-242 Me Et 0 CHF₂ 5-243 Me n-Pr 0 CHF₂ 5-244 Me i-Pr 0 CHF₂ 5-245 Me n-Bu 0 CHF₂ 5-246 Me i-Bu 0 CHF₂ 5-247 Me s-Bu 0 CHF₂ 5-248 Me t-Bu 0 CHF₂ 5-249 Me Me 1 CHF₂ 5-250 Me Et 1 CHF₂ 5-251 Me n-Pr 1 CHF₂ 5-252 Me i-Pr 1 CHF₂ 5-253 Me n-Bu 1 CHF₂ 5-254 Me i-Bu 1 CHF₂ 5-255 Me s-Bu 1 CHF₂ 5-256 Me t-Bu 1 CHF₂ 5-257 Me Me 2 CHF₂ 5-258 Me Et 2 CHF₂ 5-259 Me n-Pr 2 CHF₂ 5-260 Me i-Pr 2 CHF₂ 5-261 Me n-Bu 2 CHF₂ 5-262 Me i-Bu 2 CHF₂ 5-263 Me s-Bu 2 CHF₂ 5-264 Me t-Bu 2 CHF₂ 5-265 Et Me 0 CHF₂ 5-266 Et Et 0 CHF₂ 5-267 Et n-Pr 0 CHF₂ 5-268 Et i-Pr 0 CHF₂ 5-269 Et n-Bu 0 CHF₂ 5-270 Et i-Bu 0 CHF₂ 5-271 Et s-Bu 0 CHF₂ 5-272 Et t-Bu 0 CHF₂ 5-273 Et Me 1 CHF₂ 5-274 Et Et 1 CHF₂ 5-275 Et n-Pr 1 CHF₂ 5-276 Et i-Pr 1 CHF₂ 5-277 Et n-Bu 1 CHF₂ 5-278 Et i-Bu 1 CHF₂ 5-279 Et s-Bu 1 CHF₂ 5-280 Et t-Bu 1 CHF₂ 5-281 Et Me 2 CHF₂ 5-282 Et Et 2 CHF₂ 5-283 Et n-Pr 2 CHF₂ 5-284 Et i-Pr 2 CHF₂ 5-285 Et n-Bu 2 CHF₂ 5-286 Et i-Bu 2 CHF₂ 5-287 Et s-Bu 2 CHF₂ 5-288 Et t-Bu 2 CHF₂

B. Formulation Examples

1. Dust

A dust is obtained by mixing 10 parts by weight of a compound of the formula (I) and 90 parts by weight of talc as inert substance and comminuting the mixture in a hammer mill.

2. Dispersible Powder

A wettable powder which is readily dispersible in water is obtained by mixing 25 parts by weight of a compound of the formula (I), 64 parts by weight of kaolin-containing quartz as inert substance, 10 parts by weight of potassium lignosulfonate and 1 part by weight of sodium oleoylmethyltaurinate as wetting agent and dispersant, and grinding the mixture in a pinned-disk mill.

3. Dispersible Concentrate

A readily water-dispersible dispersion concentrate is obtained by mixing 20 parts by weight of a compound of the formula (I) with 6 parts by weight of alkylphenol polyglycol ether (®Triton X 207), 3 parts by weight of isotridecanol polyglycol ether (8 EO) and 71 parts by weight of paraffinic mineral oil (boiling range for example about 255 to above 277° C.) and grinding the mixture in a ball mill to a fineness of below 5 microns.

4. Emulsifiable Concentrate

An emulsifiable concentrate is obtained from 15 parts by weight of a compound of the formula (I), 75 parts by weight of cyclohexanone as solvent and 10 parts by weight of oxethylated nonylphenol as emulsifier.

5. Water-Dispersible Granules

Water-dispersible granules are obtained by mixing 75 parts by weight of a compound of the formula (I), 10 parts by weight of calcium lignosulfonate, 5 parts by weight of sodium lauryl sulfate, 3 parts by weight of polyvinyl alcohol and 7 parts by weight of kaolin, grinding the mixture in a pinned-disk mill, and granulating the powder in a fluidized bed by spraying on water as granulating liquid.

Water-dispersible granules are also obtained by homogenizing and precomminuting, in a colloid mill,

25 parts by weight of a compound of the formula (I), 5 parts by weight of sodium 2,2′-dinaphthylmethane-6,6′-disulfonate, 2 parts by weight of sodium oleoylmethyltaurinate, 1 part by weight of polyvinyl alcohol, 17 parts by weight of calcium carbonate and 50 parts by weight of water, subsequently grinding the mixture in a bead mill and atomizing and drying the resulting suspension in a spray tower by means of a single-fluid nozzle.

C. Biological Examples 1. Pre-Emergence Herbicidal Action Against Weed Plants

Seeds or rhizome sections of mono- and dicotyledonous weed plants are set out in pots of 9 to 13 cm in diameter, in sandy loam soil, and are covered with soil. The herbicides, formulated as emulsifiable concentrates or dusts, are applied to the surface of the covering earth in the form of aqueous dispersions or suspensions or emulsions, at a water application rate of 300 to 800 I/ha (converted) in different doses. The pots are then maintained under glass under optimum conditions for the further cultivation of the plants. After 3 to 4 weeks under optimum growth conditions under glass, the trial plants are scored for the effect of the compounds according to the invention in comparison to compounds disclosed in the prior art. As the results in the comparison tables show, the selected compounds according to the invention exhibit a better herbicidal activity against a broad spectrum of economically important monocotyledonous and dicotyledonous weeds than the compounds disclosed in the prior art.

The meanings of the abbreviations used in the comparison tables below are as follows:

ALOMY Alopecurus AMARE Amaranthus myosuroides retroflexus AVEFA Avena fatua CYPES Cyperus serotinus MATIN Matricaria inodora SETVI Setaria viridis VIOTR Viola tricolor

Comparison table 1: Pre-emergence Herbicidal action against Compound Dose [g a.c./ha] AVEFA CYPES VIOTR

80 70% 100% 90% inventive compound No. 1-153

80 40%  50% 60% compound No. 1-9, known from WO 2008/125214

Comparison table 2: Pre-emergence Dose Herbicidal [g a.c./ action against Compound ha] ALOMY CYPES

320 90% 80% inventive compound No. 3-161

320 50% 50% compound No. 3-17, known from WO 2008/125214

Comparison table 3: Pre-emergence Herbicidal Dose action against Compound [g a.c./ha] VIOTR

320 90% inventive compound No. 3-153

320 40% compound No. 3-9, known from WO 2008/125214

2. Post-Emergence Herbicidal Action Against Weed Plants

Seeds of monocotyledonous and dicotyledonous weed plants are set out in cardboard pots in sandy loam soil, covered with soil, and cultivated under glass under good growth conditions. Two to three weeks after sowing, the trial plants are treated at the three-leaf stage. The compounds according to the invention, formulated as wettable powders or as emulsifiable concentrates, are sprayed onto the surface of the green parts of the plants, at a water application rate of 600 to 800 I/ha (converted). After the trial plants have stood for 3 to 4 weeks under optimum growth conditions under glass, the action of the compounds according to the invention is scored in comparison to compounds disclosed in the prior art. As the results in the comparison tables show, the selected compounds according to the invention exhibit a better herbicidal activity against a broad spectrum of economically important monocotyledonous and dicotyledonous weeds than the compounds disclosed in the prior art.

Comparison table 4: Post-emergence Herbicidal Dose action against Compound [g a.c./ha] MATIN

80 100% inventive compound No. 1-161

80  50% compound No. 1-4, known from WO 2008/125214

Comparison table 5: Post-emergence Dose Herbicidal [g a.c./ action against Compound ha] AMARE VIOTR

320 80% 80% inventive compound No. 3-153

320 50% 40% compound No. 3-9, known from WO 2008/125214

Comparison table 6: Post-emergence Herbicidal Dose action against Compound [g a.c./ha] SETVI

80 100% inventive compound No. 3-161

80  60% compound No. 3-17, known from WO 2008/125214 

1. A 4-(4-haloalkyl-3-thiobenzoyl)pyrazole of formula (I) and/or salt thereof

in which X is (C₁-C₄)-alkyl, Y is (C₁-C₄)-haloalkyl or trifluoromethyl, R¹ is (C₁-C₄)-alkyl, R² is (C₁-C₄)-alkyl, R³ is hydrogen or (C₁-C₄)-alkyl, R⁴ is hydrogen, (C₁-C₆)-alkylsulfonyl, (C₁-C₄)-alkoxy-(C₁-C₆)-alkylsulfonyl, or is phenylsulfonyl, thiophenyl-2-sulfonyl, benzoyl, benzoyl-(C₁-C₆)-alkyl or benzyl, each of which is substituted by m identical or different radicals from the group consisting of halogen, (C₁-C₄)-alkyl, and (C₁-C₄)-alkoxy, m is 0, 1, 2 or 3, and n is 0, 1 or
 2. 2. A 4-(4-haloalkyl-3-thiobenzoyl)pyrazole and/or salt as claimed in claim 1, in which X is (C₁-C₄)-alkyl, Y is (C₁-C₄)-haloalkyl or trifluoromethyl, R¹ is (C₁-C₄)-alkyl, R² is (C₁-C₄)-alkyl, R³ is hydrogen or (C₁-C₄)-alkyl, R⁴ is hydrogen, (C₁-C₆)-alkylsulfonyl, (C₁-C₄)-alkoxy-(C₁-C₆)-alkylsulfonyl, or is phenylsulfonyl, thiophenyl-2-sulfonyl, benzoyl, benzoyl-(C₁-C₆)-alkyl or benzyl, each of which is substituted by m identical or different radicals from the group consisting of halogen, (C₁-C₄)-alkyl, and (C₁-C₄)-alkoxy, m is 0, 1, 2 or 3, and n is 0, 1 or
 2. 3. A 4-(4-haloalkyl-3-thiobenzoyl)pyrazole and/or salt as claimed in claim 1, in which X is (C₁-C₄)-alkyl, Y is trichloromethyl, difluoromethyl, dichlorofluoromethyl, chlorodifluoromethyl, pentafluoroethyl or heptafluoroisopropyl, R¹ is (C₁-C₄)-alkyl, R² is (C₁-C₄)-alkyl, R³ is hydrogen or (C₁-C₄)-alkyl, R⁴ is hydrogen, n-propylsulfonyl, methoxyethylsulfonyl, phenylsulfonyl, 4-methyl-phenylsulfonyl, or thiophenyl-2-sulfonyl, and n is 0, 1 or
 2. 4. A 4-(4-haloalkyl-3-thiobenzoyl)pyrazole and/or salt as claimed in claim 1, in which X is methyl, Y is difluoromethyl or pentafluoroethyl, R¹ is methyl, R² is methyl, R³ is hydrogen or methyl, R⁴ is hydrogen, and n is 1 or
 2. 5. A 4-(4-haloalkyl-3-thiobenzoyl)pyrazole and/or salt as claimed in claim 1, in which X is methyl, Y is pentafluoroethyl, R¹ is methyl, R² is methyl, R³ is hydrogen or methyl, R⁴ is hydrogen, and n is 1 or
 2. 6. A herbicidal composition which comprises a herbicidally effective amount of at least one compound as claimed in claim
 1. 7. The herbicidal composition as claimed in claim 6 in a mixture with at least one formulation auxiliary.
 8. The herbicidal composition as claimed in claim 6, comprising at least one further pesticidally active compound from the group of insecticides, acaricides, herbicides, fungicides, safeners, and growth regulators.
 9. The herbicidal composition as claimed in claim 6, comprising a safener.
 10. The herbicidal composition as claimed in claim 6, comprising a further herbicide.
 11. A method for controlling unwanted plants, which comprises applying an effective amount of at least one compound as claimed in claim 1 to plants and/or to a location of unwanted plant growth.
 12. A herbicidal composition as claimed in claim 6 which is capable of controlling unwanted plants.
 13. The composition as claimed in claim 12, wherein the compound of formula (I) and/or salt is capable of controlling unwanted plants in crops of useful plants.
 14. The composition as claimed in claim 13, wherein the useful plants are transgenic useful plants.
 15. A benzoic acid of formula (IIIa)

in which X is (C₁-C₄)-alkyl, Y is (C₁-C₄)-haloalkyl or trifluoromethyl, R¹ is (C₁-C₄)-alkyl, n is 0, 1 or
 2. 